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		<title>SP Hybridization</title>
		<link>https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp-hybridization/16013/</link>
					<comments>https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp-hybridization/16013/#respond</comments>
		
		<dc:creator><![CDATA[Hemant More]]></dc:creator>
		<pubDate>Wed, 08 Jun 2022 17:08:49 +0000</pubDate>
				<category><![CDATA[Physical Chemistry]]></category>
		<category><![CDATA[Axial overlap]]></category>
		<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[Covalent bond]]></category>
		<category><![CDATA[Excited state]]></category>
		<category><![CDATA[Formation of Ammonia molecule]]></category>
		<category><![CDATA[Formation of Methane molecule]]></category>
		<category><![CDATA[Formation of water molecule]]></category>
		<category><![CDATA[Geometry of molecule]]></category>
		<category><![CDATA[Ground state]]></category>
		<category><![CDATA[Hybridisation]]></category>
		<category><![CDATA[Hybridization]]></category>
		<category><![CDATA[Hybridized orbitals]]></category>
		<category><![CDATA[Hybridized state]]></category>
		<category><![CDATA[Lateral overlap]]></category>
		<category><![CDATA[Nature of chemical bond]]></category>
		<category><![CDATA[Overlapping of orbitals]]></category>
		<category><![CDATA[P-P overlap]]></category>
		<category><![CDATA[pi bond]]></category>
		<category><![CDATA[S-P overlap]]></category>
		<category><![CDATA[S-S overlap]]></category>
		<category><![CDATA[sigma bond]]></category>
		<category><![CDATA[SP hybridization]]></category>
		<category><![CDATA[SP2 hybridization]]></category>
		<category><![CDATA[SP3 hybridization]]></category>
		<category><![CDATA[Tetrahedral geometry]]></category>
		<category><![CDATA[Valence bond theory]]></category>
		<guid isPermaLink="false">https://thefactfactor.com/?p=16013</guid>

					<description><![CDATA[<p>Science &#62; Chemistry &#62; Physical Chemistry &#62; Nature of Chemical Bond &#62; sp Hybridization The mixing of one s &#8211; orbital and one p &#8211; orbital of the same atom of nearly same energy to form a set of diagonally arranged two identical hybrid orbitals of equivalent energy is called sp hybridization. These hybrid orbitals [&#8230;]</p>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp-hybridization/16013/">SP Hybridization</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
]]></description>
										<content:encoded><![CDATA[
<h5 class="wp-block-heading"><strong>Science &gt; <a href="https://thefactfactor.com/chemistry/" target="_blank" rel="noreferrer noopener">Chemistry</a> &gt; Physical Chemistry &gt; <a href="https://thefactfactor.com/chemistry/nature-of-chemical-bond/" target="_blank" rel="noreferrer noopener">Nature of Chemical Bond</a> &gt; sp Hybridization</strong></h5>



<p>The mixing of one s &#8211; orbital and one p &#8211; orbital of the same atom of nearly same energy to form a set of diagonally arranged two identical hybrid orbitals of equivalent energy is called sp hybridization. These hybrid orbitals are arranged in a linear manner around central atom and are at an angle of 180<sup>o</sup> to one another.</p>



<p class="has-accent-color has-text-color has-normal-font-size"><strong>Formation of BeF<sub>2</sub> Molecule:</strong></p>



<p><strong>Ground State of Beryllium Atom:</strong></p>



<p>Atomic number of beryllium is 4. Its configuration in ground state is 1s<sup>2</sup>, 2s<sup>2</sup>, 2p<sup>0</sup>. </p>



<p>Beryllium atom in ground state:</p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-01.png" alt="SP Hybridization" class="wp-image-19264" width="281" height="69" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-01.png 551w, https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-01-300x74.png 300w" sizes="(max-width: 281px) 100vw, 281px" /></figure>
</div>


<p><strong>Excited state of Beryllium Atom:</strong></p>



<p>During combination with fluorine, the 2s electron pair is split up and one electron is promoted to empty 2p<sub>x</sub> orbital. This condition is called excited state of beryllium. In excited state one electron of 2s migrates to 2p orbital forming 2 &#8211; half filled orbitals.<br>Beryllium atom in excited state:</p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-02.png" alt="SP Hybridization" class="wp-image-19265" width="308" height="71" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-02.png 544w, https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-02-300x69.png 300w" sizes="(max-width: 308px) 100vw, 308px" /></figure>
</div>


<p><strong>Hybridization of Beryllium Atom:</strong></p>



<p>One 2s orbital and one 2p orbitals of beryllium mix up forming two hybrid orbitals of equivalent energy. These two new equivalent orbitals are called sp hybrid orbitals. They are identical in all respect.</p>



<p>Beryllium atom in excited state:</p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-03.png" alt="SP Hybridization" class="wp-image-19266" width="245" height="78" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-03.png 406w, https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-03-300x95.png 300w" sizes="(max-width: 245px) 100vw, 245px" /></figure>
</div>


<p><strong>Angle and Geometry :</strong></p>



<p>Two sp hybridized orbitals formed, repel each other and These hybrid orbitals are arranged in a linear manner around central beryllium atom and are at an angle of 180<sup>o</sup> to one another. Each sp hybrid orbital contain unpaired electron. In each sp hybrid orbital, one of the lobes is bigger because of more concentration of electron density. Only bigger lobe is involved in bond formation.</p>



<p>Thus in BeF<sub>2</sub> molecule has linear or diagonal structure with boron atom at the centre and two fluorine atoms at the either sides of beryllium. F-Be-F bond angle is 180<sup>o</sup>.</p>



<p><strong>Bond:</strong></p>



<p>Two sp hybrid orbitals of boron atom having one unpaired electron each overlap separately with 1p orbitals of two fluorine atoms along the axis forming two covalent bonds (sigma bonds). The bonds between beryllium and fluorine are sp- p overlap. Thus F – Be — F bond angles are 180<sup>o</sup>. Molecule is diagonal or linear. Both Be-F bonds in beryllium difluoride are of equal strength.</p>



<p><strong>Diagram:</strong></p>


<div class="wp-block-image">
<figure class="aligncenter size-full"><img loading="lazy" decoding="async" width="387" height="60" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-04.png" alt="SP Hybridization" class="wp-image-19269" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-04.png 387w, https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-04-300x47.png 300w" sizes="auto, (max-width: 387px) 100vw, 387px" /></figure>
</div>


<p><strong>Type and Geometry of Beryllium difluoride Molecule:</strong></p>



<figure class="wp-block-table aligncenter is-style-stripes"><table><tbody><tr><td>Name of Molecule</td><td>Beryllium difluoride</td></tr><tr><td>Molecular Formula</td><td>BeF<sub>2</sub></td></tr><tr><td>Type Of Hybridisation</td><td>Sp</td></tr><tr><td>Geometry</td><td>Diagonal or Linear</td></tr><tr><td>No. Of Bonds</td><td>2</td></tr><tr><td>No. Of Sigma bonds</td><td>2 sigma</td></tr><tr><td>Bond angle</td><td>180<sup>0</sup></td></tr><tr><td>Overlaps</td><td>2 sp &#8211; p</td></tr><tr><td>Bonds</td><td>2 Be-F</td></tr></tbody></table></figure>



<p class="has-accent-color has-text-color has-normal-font-size"><strong>BeF<sub>2</sub> Is linear molecule, while H<sub>2</sub>O is angular molecule.</strong></p>



<p>In BeF<sub>2</sub> molecule, beryllium undergoes sp hybridization and achieve electronic configuration 1s<sup>2</sup>, 2s<sup>1</sup>2p<sub>x</sub><sup>1</sup>&nbsp;in excited state. During formation of beryllium difluoride boron undergoes sp hybridization One 2s orbital and one 2p orbital of beryllium mix up forming two hybrid orbitals of equivalent energy. These two new equivalent orbitals are called sp hybrid orbitals. They are identical in all respect. Two sp hybridized orbitals formed, repel each other and they are directed diagonally opposite in space.&nbsp; Angle between them is 180<sup>0</sup>. Two sp hybrid orbitals of boron atom having one unpaired electron each overlap separately with 1p orbitals of two fluorine atoms along the axis forming two covalent bonds (sigma bonds). Thus BeF<sub>2</sub> Is linear molecule.</p>



<p>In water, the oxygen atom is sp<sup>3</sup> hybridized. Two hybrid orbitals have paired electrons (lone pair) and they are non &#8211; bonding orbitals.&nbsp; Other two orbitals are half &#8211; filled (singly occupied) and they are bonding orbitals. These hybridized orbitals are in four directions of four corners of tetrahedron. Four sp<sup>3</sup> hybridized orbitals formed, repel each other and they should be directed towards the four corners of a regular&nbsp; tetrahedron and&nbsp; Angle between them should be 109.5<sup>0</sup>.&nbsp; The non bonding electron repel each other strongly and occupy more space than the electron pairs involved in bonding.&nbsp; The force of repulsion between electron pair decreases in following order. lone pair – lone pair &gt; lone pair- bond pair &gt;&nbsp; bond pair – bond pair. Hence the bond angle between two lone pairs i.e. H-O-H angle decreases from109.5<sup>0</sup>&nbsp;to 104.5<sup>0</sup>. Thus water molecule is angular.</p>



<p class="has-accent-color has-text-color has-normal-font-size"><strong>Formation of acetylene (C<sub>2</sub>H <sub>2</sub>) Molecule:</strong></p>



<p id="block-11dc139b-e6fb-4f76-8590-c1e24e0fdf47"><strong>Ground State of Carbon Atom:<br></strong>Atomic number of carbon is 6. Its configuration in ground state is 1s<sup>2</sup>, 2s<sup>2</sup>, 2p<sup>2</sup> i.e. 1s<sup>2</sup> 2s<sup>2</sup>, 2p<sub>x</sub><sup>1 </sup>2p<sub>y</sub><sup>1 </sup>2p<sub>z</sub><sup>0</sup></p>



<p>Carbon atom in ground state:</p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img loading="lazy" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-06.png" alt="" class="wp-image-19250" width="331" height="85" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-06.png 544w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-06-300x77.png 300w" sizes="auto, (max-width: 331px) 100vw, 331px" /></figure>
</div>


<p><strong>Excited state <strong>of Carbon Atom</strong>:</strong></p>



<p>During combination with hydrogen, the 2s electron pair is split up and one electron is promoted to empty 2p<sub>z</sub> orbital. This condition is called excited state of carbon. In excited state one electron of 2s migrates to 2p orbital forming 4 &#8211; half filled orbitals.<br>Carbon atom in excited state: </p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img loading="lazy" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-07.png" alt="" class="wp-image-19251" width="336" height="83" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-07.png 545w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-07-300x74.png 300w" sizes="auto, (max-width: 336px) 100vw, 336px" /></figure>
</div>


<p><strong>Hybridization:</strong></p>



<p>In acetylene there is sp hybridization. One 2s orbital and one 2p orbitals of carbon mix up forming two hybrid orbitals of equivalent energy. These two new equivalent orbitals are called sp hybrid orbitals. They are identical in all respect. Two ‘p’ orbitals of each carbon atom remains unhybridized.</p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img loading="lazy" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-05.png" alt="" class="wp-image-19273" width="301" height="82" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-05.png 483w, https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-05-300x81.png 300w" sizes="auto, (max-width: 301px) 100vw, 301px" /></figure>
</div>


<p><strong>Angle and Geometry:</strong></p>



<p>Two sp hybridized orbitals formed, repel each other and These hybrid orbitals are arranged along x- axis in a linear manner around central carbon atom and are at an angle of 180<sup>0</sup> to one another. The unhybridized p<sub>y</sub> and p<sub>z</sub> orbital remain perpendicular to hybrid orbitals along y-axis and z- axis ,<br>mutually perpendicular. Each sp hybrid orbital and unhybrid orbitals contain unpaired electron. In each sp hybrid orbital, one of the lobes is bigger because of more concentration of electron density. Only bigger lobe is involved in bond formation.</p>



<p>As all the four atoms in C<sub>2</sub>H<sub>2 </sub>molecule being in the same line, the molecule is diagonal or linear. H-C-C bond angle is 180<sup>o</sup>.</p>



<p><strong>Formation of Bonds:</strong></p>



<ol class="wp-block-list"><li><strong>Sigma Bond Formation :</strong></li></ol>



<p>A covalent bond formed by collinear or coaxial or in the line of internuclear axis. Overlapping of orbitals is known as sigma bond. One Sp hybrid orbital of one carbon atom overlaps with One hybrid orbital of other carbon atom by head on collision forming sigma bond. One (Sp- Sp ) overlap. Remaining one hybrid orbitals of each carbon atom overlap with ‘s’ orbital of two hydrogen atoms separately forming two sigma bonds. (2 C – H). Two (Sp– s)overlaps. Both C-H bond in Acetylene are of equal strength. Thus there are Three sigma bonds. Sigma bonds are stronger.</p>



<p><strong>2) Formation of pi Bond :<br></strong>The covalent bond formed by collateral or sidewise overlapping is called pi bond. The unhybridized 2 p<sub>x</sub> and 2 p<sub>z</sub> orbitals of each carbon atom being perpendicular to each other and to the plane of H-C-C-H axis overlap laterally with one another to form two week pi bond between two<br>carbon atoms by two p &#8211; p overlap. (one 2 p<sub>y</sub> -2 p<sub>y</sub> )and (one 2p<sub>z</sub>-2 p<sub>z</sub>) . Thus two (p-p) -overlaps.</p>



<p>In ethylene molecule there are 3 sigma bonds and 2 pi bonds. There is a triple bond between carbon and carbon consisting one sigma and two pi bonds.</p>



<p><strong>Diagram:</strong></p>


<div class="wp-block-image">
<figure class="aligncenter size-full"><img loading="lazy" decoding="async" width="251" height="177" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP-Hybridized-Orbitals-06.png" alt="" class="wp-image-19274"/></figure>
</div>


<p><strong>Type and Geometry of Acetylene Molecule:</strong></p>



<figure class="wp-block-table aligncenter is-style-stripes"><table><tbody><tr><td>Name of Molecule</td><td>Acetylene</td></tr><tr><td>Molecular Formula</td><td>C2H2</td></tr><tr><td>Type Of Hybridisation</td><td>Sp</td></tr><tr><td>Geometry</td><td>Diagonal or Linear</td></tr><tr><td>No. Of Bonds</td><td>5</td></tr><tr><td>No. Of Sigma bonds</td><td>3</td></tr><tr><td>No. of pi Bonds</td><td>1</td></tr><tr><td>Overlaps</td><td>One (Sp- Sp) &#8211; s bond <br>Two (Sp– s) &#8211; s bond <br>Two (p-p) &#8211; p bond</td></tr><tr><td>Bond angle</td><td>H-C-C 1800</td></tr><tr><td>Bonds</td><td>C-H Single Bond (2 sigma) <br>C-C Tripple bond (1 sigma and 2 pi)</td></tr></tbody></table></figure>



<p><strong>There is only one pi bond in ethylene molecule but there are two pi bonds in the acetylene molecule:</strong></p>



<p>In ethylene molecule carbon atom shows sp<sup>2</sup> hybridization in excited state. The resulting three hybrid orbitals form two C-H bonds and One pi bond of sigma type. Thus each carbon atom is left with unhybridized p<sub>z</sub> orbitals with lobes above and below the plane of hybridized orbitals. These two unhybridized orbitals overlap each other laterally and form a single pi bond between two carbon atoms.</p>



<p>In acetylene molecule carbon atom shows sp hybridization in excited state. The resulting two orbitals are linear and form one C-H bond and one C-C bond of sigma type. Thus each carbon is left with two unhybridized p<sub>y</sub> and p<sub>z</sub> orbitals, which are mutually perpendicular to H-C-C-H axis. These unhybridized orbitals overlap each other laterally and form two pi bonds between two carbon atoms.</p>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp-hybridization/16013/">SP Hybridization</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
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			</item>
		<item>
		<title>SP2 Hybridization</title>
		<link>https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp2-hybridization/16168/</link>
					<comments>https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp2-hybridization/16168/#respond</comments>
		
		<dc:creator><![CDATA[Hemant More]]></dc:creator>
		<pubDate>Wed, 08 Jun 2022 14:11:01 +0000</pubDate>
				<category><![CDATA[Physical Chemistry]]></category>
		<category><![CDATA[Axial overlap]]></category>
		<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[Covalent bond]]></category>
		<category><![CDATA[Excited state]]></category>
		<category><![CDATA[Formation of Ammonia molecule]]></category>
		<category><![CDATA[Formation of Methane molecule]]></category>
		<category><![CDATA[Formation of water molecule]]></category>
		<category><![CDATA[Geometry of molecule]]></category>
		<category><![CDATA[Ground state]]></category>
		<category><![CDATA[Hybridisation]]></category>
		<category><![CDATA[Hybridization]]></category>
		<category><![CDATA[Hybridized orbitals]]></category>
		<category><![CDATA[Hybridized state]]></category>
		<category><![CDATA[Lateral overlap]]></category>
		<category><![CDATA[Nature of chemical bond]]></category>
		<category><![CDATA[Overlapping of orbitals]]></category>
		<category><![CDATA[P-P overlap]]></category>
		<category><![CDATA[pi bond]]></category>
		<category><![CDATA[S-P overlap]]></category>
		<category><![CDATA[S-S overlap]]></category>
		<category><![CDATA[sigma bond]]></category>
		<category><![CDATA[SP hybridization]]></category>
		<category><![CDATA[SP2 hybridization]]></category>
		<category><![CDATA[SP3 hybridization]]></category>
		<category><![CDATA[Tetrahedral geometry]]></category>
		<category><![CDATA[Valence bond theory]]></category>
		<guid isPermaLink="false">https://thefactfactor.com/?p=16168</guid>

					<description><![CDATA[<p>Science &#62; Chemistry &#62; Physical Chemistry &#62; Nature of Chemical Bond &#62; sp2 Hybridization Mixing of one &#8216;s&#8217; orbital and two &#8216;p&#8217; &#8211; orbitals of nearly same energy forming set of trigonally arranged three&#160;identical orbitals of equal energy is known as sp2&#160;hybridization. Geometry sp2&#160;Hybridization: The hybrid orbitals are arranged around the central atom in a [&#8230;]</p>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp2-hybridization/16168/">SP2 Hybridization</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
]]></description>
										<content:encoded><![CDATA[
<h5 class="wp-block-heading"><strong>Science &gt; <a href="https://thefactfactor.com/chemistry/" target="_blank" rel="noreferrer noopener">Chemistry</a> &gt; Physical Chemistry &gt; <a href="https://thefactfactor.com/chemistry/nature-of-chemical-bond/" target="_blank" rel="noreferrer noopener">Nature of Chemical Bond</a> &gt; sp2 Hybridization</strong></h5>



<p>Mixing of one &#8216;s&#8217; orbital and two &#8216;p&#8217; &#8211; orbitals of nearly same energy forming set of trigonally arranged three&nbsp;identical orbitals of equal energy is known as sp<sup>2</sup>&nbsp;hybridization.</p>



<p><strong>Geometry sp<sup>2</sup>&nbsp;Hybridization:</strong></p>



<p>The hybrid orbitals are arranged around the central atom in a plane at an angle of 120°&nbsp;to one another. When these three&nbsp;orbitals overlap with appropriate orbitals of three other atoms, three bonds are formed and the resulting&nbsp;molecule has a trigonal planar structure. Each bond angle is 120°.</p>



<p><strong>Diagram</strong>:</p>


<div class="wp-block-image">
<figure class="aligncenter size-full"><img loading="lazy" decoding="async" width="430" height="135" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-01.png" alt="SP2 Hybridization" class="wp-image-19240" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-01.png 430w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-01-300x94.png 300w" sizes="auto, (max-width: 430px) 100vw, 430px" /></figure>
</div>


<p class="has-accent-color has-text-color has-normal-font-size"><strong>Formation of Boron Trifluoride Molecules:</strong></p>



<p class="has-primary-color has-text-color has-normal-font-size"><strong>Ground State of Boron Atom:</strong></p>



<p>Atomic number of boron is 5. Its configuration in ground state is 1s<sup>2</sup>, 2s<sup>2</sup>, 2p<sup>1</sup></p>



<p>Boron atom in ground state:</p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img loading="lazy" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-02.png" alt="SP2 Hybridization" class="wp-image-19241" width="306" height="74" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-02.png 857w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-02-300x73.png 300w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-02-768x187.png 768w" sizes="auto, (max-width: 306px) 100vw, 306px" /></figure>
</div>


<p><strong>Excited State <strong>of Boron Atom</strong>:</strong></p>



<p>During combination with fluorine, the 2s electron pair is split up and one electron is promoted to empty&nbsp;2p<sub>y</sub> orbital. This condition is called excited state of boron. In excited state one electron of 2s migrates&nbsp;to 2p orbital forming 3 &#8211; half filled orbitals.</p>



<p>Boron atom in excited state:</p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img loading="lazy" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-03.png" alt="SP2 Hybridization" class="wp-image-19242" width="319" height="72" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-03.png 865w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-03-300x68.png 300w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-03-768x174.png 768w" sizes="auto, (max-width: 319px) 100vw, 319px" /></figure>
</div>


<p><strong>Hybridization <strong>of Boron Atom</strong>:<br></strong>One 2s orbital and two 2p orbitals of boron mix up forming three hybrid orbitals of equivalent energy.&nbsp;These three new equivalent orbitals are called sp<sup>2&nbsp;</sup>hybrid orbitals. They are identical in all respect</p>



<p>Boron atom in hybridized state:</p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img loading="lazy" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-04.png" alt="SP2 Hybridization" class="wp-image-19244" width="290" height="76" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-04.png 469w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-04-300x79.png 300w" sizes="auto, (max-width: 290px) 100vw, 290px" /></figure>
</div>


<p><strong>Angle and Geometry:</strong></p>



<ul class="wp-block-list" id="block-1f0ddf0d-6230-4b06-bbd5-1660982ae5a7"><li>Three sp<sup>2&nbsp;</sup>hybridized orbitals formed, repel each other and they are directed towards the three corners&nbsp;of an equilateral triangle. The angle between them is 120°.</li><li>Each sp<sup>2&nbsp;</sup>hybrid orbital contains an unpaired electron.</li><li>In each sp<sup>2&nbsp;</sup>hybrid orbital, one of the lobes is bigger because of more concentration of electron density.&nbsp;Only bigger lobe is involved in bond formation.</li><li>Thus BF<sub>3</sub> molecule has a trigonal planar structure with boron atom at the centre and three fluorine&nbsp;atoms at the four corners of equilateral triangle. F-B-F bond angle is 120°.</li></ul>



<p><strong>Bond Formation:</strong></p>



<p>Three sp<sup>2</sup> hybrid orbitals of boron atom having one unpaired electron each overlap separately with 2p orbitals of three fluorine atoms along the axis forming three covalent bonds (sigma). Thus in BF<sub>3</sub> molecule has a planar structure with a boron atom at the centre and three fluorine atoms at the three corners of an equilateral triangle. F-B-F bond angle is 120°.</p>



<p><strong>Bond:</strong></p>



<ul class="wp-block-list" id="block-0b05754e-38db-4ac1-9abf-c91209035ad1"><li>There are three sigma bonds..</li><li>The bonds between boron and fluorine are sp<sup>2</sup>&#8211; p.</li><li>Thus F – B — F bond angles are 120°. The molecule is trigonal planar.</li><li>All B-F bonds in boron trifluoride are of equal strength.</li></ul>



<p><strong>Diagram:</strong></p>


<div class="wp-block-image">
<figure class="aligncenter size-full"><img loading="lazy" decoding="async" width="245" height="206" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-05.png" alt="SP2 Hybridization" class="wp-image-19246"/></figure>
</div>


<h4 class="wp-block-heading" id="block-fe46bc6e-8caa-47bb-bff3-cf8f1528a8ad"><br>Type and Geometry of Boron trifluoride Molecule:<br>﻿</h4>



<figure class="wp-block-table aligncenter is-style-stripes"><table><tbody><tr><td>Name of Molecule</td><td>Boron trifluoride</td></tr><tr><td>Molecular Formula</td><td>BF<sub>3</sub></td></tr><tr><td>Type Of Hybridization</td><td>sp<sup>2</sup></td></tr><tr><td>Geometry</td><td>Trigonal planar</td></tr><tr><td>No. Of Bonds</td><td>3</td></tr><tr><td>No. Of Sigma bonds</td><td>3 sigma</td></tr><tr><td>Bond angle</td><td>120<sup>0</sup></td></tr><tr><td>Overlaps</td><td>3 sp<sup>2</sup> &#8211; p</td></tr><tr><td>Bonds</td><td>3 B-F</td></tr></tbody></table></figure>



<p><strong>The BF<sub>3</sub>&nbsp;molecule has a planar structure while NH<sub>3</sub>&nbsp;molecule has a pyramidal structure.<br></strong>During formation of boron trifluoride, boron undergoes sp<sup>2</sup> hybridization and achieve the electronic configuration&nbsp;1s<sup>2</sup>, 2s<sup>1</sup>2p<sub>x</sub><sup>1</sup>2p<sub>y</sub><sup>1</sup>. In the excited state, one 2s orbital and two 2p orbitals of boron mix up forming three hybrid orbitals of equivalent energy.&nbsp;These three new equivalent orbitals are called sp<sup>2</sup> hybrid orbitals. They are identical in all respect. Three sp<sup>2</sup> hybridized orbitals formed, repel each other and they are directed towards the three corners of an equilateral triangle (in one plane). Angle between them is 120<sup>o</sup>. Three sp<sup>2</sup> hybrid orbitals of boron atom having one unpaired electron each overlap separately with 1p orbitals of three fluorine atoms along the axis forming three covalent bonds (sigma bonds). Thus boron trifluoride has triangular planar structure.</p>



<p>During formation of ammonia nitrogen undergoes sp<sup>3</sup> hybridization. One 2s orbital and three 2p orbitals of mix up forming four hybrid orbitals of equivalent energy. These four new equivalent orbitals are called sp<sup>3</sup> hybrid orbitals. They are identical in all respect and they should be directed towards the four corners of a regular tetrahedron and Angle between them should be 109.5<sup>o</sup>. Three hybridized orbitals contain unpaired electron. The fourth hybridized orbital has lone pair of electron. The three half filled (containing unpaired electron) sp<sup>3</sup> hybrid orbitals of nitrogen overlap axially with three half filled 1s orbitals of three hydrogen atoms separately to form three covalent N-H bonds (sigma bonds). The fourth hybrid orbital containing lone pair of electron remains non bonded. The non bonding electron repel each other strongly and occupy more space than the electron pairs involved in bonding. The force of repulsion between lone pair- bond pair is greater than bond pair – bond pair. Hence the<br>bond angle i.e. H-N-H angle decreases from109.5<sup>o</sup> to 107<sup>o</sup>.</p>



<p class="has-accent-color has-text-color has-normal-font-size"><strong>Formation of Ethylene Molecule:</strong></p>



<p id="block-11dc139b-e6fb-4f76-8590-c1e24e0fdf47"><strong>Ground State of Carbon Atom:<br></strong>Atomic number of carbon is 6. Its configuration in ground state is 1s<sup>2</sup>, 2s<sup>2</sup>, 2p<sup>2</sup> i.e. 1s<sup>2</sup> 2s<sup>2</sup>, 2p<sub>x</sub><sup>1 </sup>2p<sub>y</sub><sup>1 </sup>2p<sub>z</sub><sup>0</sup></p>



<p>Carbon atom in ground state:</p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img loading="lazy" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-06.png" alt="" class="wp-image-19250" width="331" height="85" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-06.png 544w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-06-300x77.png 300w" sizes="auto, (max-width: 331px) 100vw, 331px" /></figure>
</div>


<p><strong>Excited state <strong>of Carbon Atom</strong>:</strong></p>



<p>During combination with hydrogen, the 2s electron pair is split up and one electron is promoted to empty 2p<sub>z</sub> orbital. This condition is called excited state of carbon. In excited state one electron of 2s migrates to 2p orbital forming 4 &#8211; half filled orbitals.<br>Carbon atom in excited state: </p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img loading="lazy" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-07.png" alt="" class="wp-image-19251" width="336" height="83" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-07.png 545w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-07-300x74.png 300w" sizes="auto, (max-width: 336px) 100vw, 336px" /></figure>
</div>


<p><strong>Hybridization <strong>of Carbon Atom</strong>:</strong></p>



<p>In ethylene there is sp<sup>2</sup> hybridization. One 2s orbital and two 2p orbitals of carbon mix up forming three hybrid orbitals of equivalent energy. These three new equivalent orbitals are called sp<sup>2</sup> hybrid orbitals. They are identical in all respect. One ‘p’ orbital of each carbon atom remains unhybridized</p>



<p>Carbon atom in hybridized state:</p>


<div class="wp-block-image">
<figure class="aligncenter size-full is-resized"><img loading="lazy" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-08.png" alt="" class="wp-image-19252" width="290" height="85" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-08.png 527w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-08-300x88.png 300w" sizes="auto, (max-width: 290px) 100vw, 290px" /></figure>
</div>


<p><strong>Angle and Geometry:</strong></p>



<p>Three sp<sup>2</sup> hybridized orbitals formed, repel each other and they are directed in a plane towards the three corners of an equilateral triangle. Angle between them is 120<sup>o</sup>. The unhybridized p<sub>z</sub> orbital remain perpendicular to this plane. Each sp<sup>2</sup> hybrid orbital contain unpaired electron. In each sp<sup>2</sup> hybrid orbital, one of the lobes is bigger because of more concentration of electron density. Only bigger lobe is involved in bond formation.</p>



<p>As all the six atoms in C<sub>2</sub>H<sub>6</sub> molecule being in the same plane, the molecule is planar. H-C-H bond angle is 120<sup>o</sup>. H-C-C bond angle is 120<sup>o</sup>.</p>



<p><strong>Bonds Formation:<br>1. Sigma Bond Formation :</strong></p>



<p>A covalent bond formed by collinear or coaxial or in the line of internuclear axis. Overlapping of orbitals is known as sigma bond. One Sp<sup>2</sup> hybrid orbital of one carbon atom overlaps with One hybrid orbital of other carbon atom by head on collision forming sigma bond. One (Sp<sup>2</sup>&#8211; Sp<sup>2</sup> ) overlap.</p>



<p>Remaining two hybrid orbitals of each carbon atom overlap with ‘s’ orbital of four hydrogen atoms separately forming four sigma bonds. (C – H). Four (Sp<sup>2</sup>– s) overlaps. All C-H bond in ethylene are of equal strength.</p>



<p>Thus there are five sigma bonds. Sigma bonds are stronger.</p>



<p><strong>2. Formation of pi Bond:</strong></p>



<p>The covalent bond formed by collateral or sidewise overlapping is called pi bond. The unhybridized 2 p<sub>z</sub> orbitals of each carbon atom being  perpendicular to the plane of four hydrogen atoms and carbon atoms overlap laterally with one another to form a week pi bond between two carbon atoms by p &#8211; p overlap. One (p-p) -pi bond. This bond consists of two equal electron cloud one lying above the plane of the atom and other lying below this plane. </p>



<p>Hence, in ethylene molecule there are 5 sigma bonds and 1 pi bond.</p>



<p><strong>Diagram :</strong></p>


<div class="wp-block-image">
<figure class="aligncenter size-full"><img loading="lazy" decoding="async" width="385" height="131" src="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-09.png" alt="" class="wp-image-19256" srcset="https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-09.png 385w, https://thefactfactor.com/wp-content/uploads/2022/06/SP2-Hybridized-Orbitals-09-300x102.png 300w" sizes="auto, (max-width: 385px) 100vw, 385px" /></figure>
</div>


<p><strong>Type and Geometry of Ethylene Molecule :</strong></p>



<figure class="wp-block-table aligncenter is-style-stripes"><table><tbody><tr><td>Name of Molecule</td><td>Ethylene</td></tr><tr><td>Molecular Formula</td><td>C<sub>2</sub>H<sub>4</sub></td></tr><tr><td>Type Of Hybridisation</td><td>Sp<sup>2</sup></td></tr><tr><td>Geometry</td><td>Trigonal planar</td></tr><tr><td>No. Of Bonds</td><td>6</td></tr><tr><td>No. Of Sigma bonds</td><td>5 sigma</td></tr><tr><td>No. of pi Bonds</td><td>1</td></tr><tr><td>Overlaps</td><td>One (Sp<sup>2</sup>&#8211; Sp<sup>2</sup> ) &#8211; sigma bond <br>Four (Sp<sup>2</sup>– s) &#8211; sigma bond <br>One (p-p) &#8211; pi bond</td></tr><tr><td>Bond angle</td><td>H-C-C  120<sup>0</sup> and H-C-H  120<sup>0</sup></td></tr><tr><td>Overlaps</td><td>4 sp3 &#8211; s</td></tr><tr><td>Bonds</td><td>4 C-H Single Bond ( 4 sigma) <br>1 C-C Double bond ( 1 sigma 1 pi)</td></tr></tbody></table></figure>



<p></p>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp2-hybridization/16168/">SP2 Hybridization</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
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		<title>sp3 Hybridization</title>
		<link>https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp3-hybridization/11008/</link>
					<comments>https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp3-hybridization/11008/#comments</comments>
		
		<dc:creator><![CDATA[Hemant More]]></dc:creator>
		<pubDate>Wed, 01 Apr 2020 06:17:31 +0000</pubDate>
				<category><![CDATA[Physical Chemistry]]></category>
		<category><![CDATA[Axial overlap]]></category>
		<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[Covalent bond]]></category>
		<category><![CDATA[Excited state]]></category>
		<category><![CDATA[Formation of Ammonia molecule]]></category>
		<category><![CDATA[Formation of Methane molecule]]></category>
		<category><![CDATA[Formation of water molecule]]></category>
		<category><![CDATA[Geometry of molecule]]></category>
		<category><![CDATA[Ground state]]></category>
		<category><![CDATA[Hybridisation]]></category>
		<category><![CDATA[Hybridization]]></category>
		<category><![CDATA[Hybridized orbitals]]></category>
		<category><![CDATA[Hybridized state]]></category>
		<category><![CDATA[Lateral overlap]]></category>
		<category><![CDATA[Nature of chemical bond]]></category>
		<category><![CDATA[Overlapping of orbitals]]></category>
		<category><![CDATA[P-P overlap]]></category>
		<category><![CDATA[pi bond]]></category>
		<category><![CDATA[S-P overlap]]></category>
		<category><![CDATA[S-S overlap]]></category>
		<category><![CDATA[sigma bond]]></category>
		<category><![CDATA[SP hybridization]]></category>
		<category><![CDATA[SP2 hybridization]]></category>
		<category><![CDATA[SP3 hybridization]]></category>
		<category><![CDATA[Tetrahedral geometry]]></category>
		<category><![CDATA[Valence bond theory]]></category>
		<guid isPermaLink="false">https://thefactfactor.com/?p=11008</guid>

					<description><![CDATA[<p>Science &#62; Chemistry &#62; Physical Chemistry &#62; Nature of Chemical Bond &#62; sp3 Hybridization The mixing of one s-orbital and three p- orbitals of the same atom having nearly&#160;the same energy to form four orbitals of equal in all respects and tetrahedrally arranged is known as sp3 hybridization. Geometry of sp3 Hybridization: sp3 hybridized orbitals [&#8230;]</p>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp3-hybridization/11008/">sp3 Hybridization</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
]]></description>
										<content:encoded><![CDATA[
<h5 class="wp-block-heading"><strong>Science &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/" target="_blank">Chemistry</a> &gt; Physical Chemistry &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/nature-of-chemical-bond/" target="_blank">Nature of Chemical Bond</a> &gt; sp3 Hybridization</strong></h5>



<p>The mixing of one s-orbital and three p- orbitals of the same atom having nearly&nbsp;the same energy to form four orbitals of equal in all respects and tetrahedrally arranged is known as sp3 hybridization.</p>



<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Geometry of sp3 Hybridization:</strong></p>



<p>sp<sup>3</sup> hybridized orbitals repel each other and they are directed to four corners of a regular tetrahedron. The angle between them is 109.5° and the geometry of the molecule is tetrahedral (non-planar). This type of hybridization is also known as tetrahedral hybridization. The sp<sup>3</sup> hybridization is shown pictorially in the figure.</p>



<figure class="wp-block-image size-large"><img loading="lazy" decoding="async" width="542" height="150" src="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-06.png" alt="SP3 Hybridization" class="wp-image-11002" srcset="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-06.png 542w, https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-06-300x83.png 300w" sizes="auto, (max-width: 542px) 100vw, 542px" /></figure>



<p class="has-luminous-vivid-orange-color has-very-light-gray-background-color has-text-color has-background has-medium-font-size"><strong>Formation of Methane&nbsp;Molecule&nbsp;(</strong> <strong>CH<sub>4</sub> ):</strong></p>



<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Step
-1: Formation of the excited state of a Carbon atom:</strong></p>



<p>The carbon atom in the ground state takes up some energy and goes to the excited state.&nbsp; In this process, a pair of electrons in 2s orbital splits up and one of the electron from this pair is transferred to empty 2pz orbital.&nbsp; Thus the excited state has four half-filled orbitals.</p>


<div class="wp-block-image">
<figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="150" src="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-04.png" alt="SP3 Hybridization" class="wp-image-11000"/></figure>
</div>


<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Step &#8211; 2: Hybridization of Orbitals:</strong></p>



<p>One orbital
of 2s and three orbitals of 2p mix up forming four hybrid orbitals of
equivalent energy. These four new equivalent orbitals are called sp<sup>3</sup>
hybrid orbitals. They are identical in all respect.</p>


<div class="wp-block-image">
<figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="325" height="105" src="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-05.png" alt="SP3 Hybridization" class="wp-image-11001" srcset="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-05.png 325w, https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-05-300x97.png 300w" sizes="auto, (max-width: 325px) 100vw, 325px" /></figure>
</div>


<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Angle and Geometry:</strong></p>



<p>Four sp<sup>3</sup>&nbsp;hybridized
orbitals formed, repel each other and they are directed towards the four
corners of a regular tetrahedron. &nbsp; &nbsp;The&nbsp;Angle between them is
109.5°. Each sp<sup>3</sup> hybrid orbital contains one unpaired electron.</p>



<p>In each sp<sup>3</sup> hybrid orbital, one of the lobes is bigger because of more concentration of electron density. Only a bigger lobe is involved in bond formation. Due to this maximum overlapping is achieved. </p>



<p>Four sp<sup>3</sup>
hybrid orbitals of carbon atom having one unpaired electron each overlap
separately with 1s orbitals of four hydrogen atom along the axis forming four
covalent bonds. Thus in CH<sub>4</sub> molecule has a tetrahedral structure
with a carbon atom at the centre and four hydrogens at the four corners of a
regular tetrahedron. H-C-H bond angle is 109.5°.</p>



<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Bonds:</strong></p>



<p>Four sp<sup>3</sup> hybrid orbitals of carbon atom having one unpaired electron each overlap separately with 1s orbitals of four hydrogen atom along the axis forming four covalent bonds (sigma bonds). The bonds between carbon and hydrogen are sp<sup>3</sup>&#8211; s. Thus H – C – H bond angles are 109.5°. The molecule is tetrahedral. All C-H bonds in methane are of equal strength.</p>


<div class="wp-block-image">
<figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="685" height="153" src="https://thefactfactor.com/wp-content/uploads/2020/04/Hybridization-of-Orbitals-08.png" alt="Formation of Methane Molecule" class="wp-image-11010" srcset="https://thefactfactor.com/wp-content/uploads/2020/04/Hybridization-of-Orbitals-08.png 685w, https://thefactfactor.com/wp-content/uploads/2020/04/Hybridization-of-Orbitals-08-300x67.png 300w" sizes="auto, (max-width: 685px) 100vw, 685px" /></figure>
</div>


<p><strong>Type and Geometry of Methane Molecule:</strong></p>


<table border="1" align="center" width="60%">
<tbody>
<tr>
<td width="188">
<p>Name of Molecule</p>
</td>
<td width="100">
<p>Methane</p>
</td>
</tr>
<tr>
<td width="188">
<p>Molecular Formula</p>
</td>
<td width="100">
<p>CH<sub>4</sub></p>
</td>
</tr>
<tr>
<td width="188">
<p>Type Of Hybridization</p>
</td>
<td width="100">
<p>sp<sup>3</sup></p>
</td>
</tr>
<tr>
<td width="188">
<p>Geometry</p>
</td>
<td width="100">
<p>Tetrahedral</p>
</td>
</tr>
<tr>
<td width="188">
<p>No. Of Bonds</p>
</td>
<td width="100">
<p>4</p>
</td>
</tr>
<tr>
<td width="188">
<p>No. Of Sigma bonds</p>
</td>
<td width="100">
<p>4 sigma</p>
</td>
</tr>
<tr>
<td width="188">
<p>Bond angle</p>
</td>
<td width="100">
<p>109.5°</p>
</td>
</tr>
<tr>
<td width="188">
<p>Overlaps</p>
</td>
<td width="100">
<p>4 sp<sup>3</sup> &#8211; s</p>
</td>
</tr>
<tr>
<td width="188">
<p>Bonds</p>
</td>
<td width="100">
<p>4 C-H</p>
</td>
</tr>
</tbody>
</table>


<p class="has-luminous-vivid-orange-color has-very-light-gray-background-color has-text-color has-background has-medium-font-size"><strong>Formation of Ammonia Molecule (</strong> <strong>NH<sub>3</sub>):</strong></p>



<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Need of Hybridization in Ammonia Molecule:</strong></p>



<p>In nitrogen atom, there are three half-filled 2p orbitals and the&nbsp;valency should be 3 and it is three. These three ‘p’ orbitals are perpendicular to each other and if they form bonds, the angle between them should be 90°. But the actual angle between bonding orbitals in ammonia is 107°. To explain this difference in the angle the concept of hybridization is required.</p>



<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Electron Configuration:</strong></p>



<p>The Atomic
number of Nitrogen is 7.&nbsp; Its configuration in ground state is 1s<sup>2</sup>,
2s<sup>2</sup>, 2p<sup>3</sup></p>


<div class="wp-block-image">
<figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="65" src="https://thefactfactor.com/wp-content/uploads/2020/04/SP3-Hybridization-02.png" alt="SP3 Hybridization" class="wp-image-11012"/></figure>
</div>


<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Hybridization:</strong></p>



<p>In the formation of ammonia one 2s orbital and three 2p orbitals of nitrogen mix up forming four hybrid orbitals of equivalent energy. These four new equivalent orbitals are called sp<sup>3</sup> hybrid orbitals. They are identical in all respect. One hybrid orbital has paired electrons (lone pair) and it is nonbonding orbital. The other three orbitals are half-filled and they are bonding orbitals. The nonbonding pair of hybridized orbitals is called as a lone pair. These hybridized orbitals are in the directions of four corners of a regular tetrahedron.</p>


<div class="wp-block-image">
<figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="63" src="https://thefactfactor.com/wp-content/uploads/2020/04/SP3-Hybridization-03.png" alt="SP3 Hybridization" class="wp-image-11013"/></figure>
</div>


<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Angle and Geometry:</strong></p>



<p>Four sp<sup>3&nbsp;</sup>hybridized orbitals formed, repel each other and they should be directed towards the four corners of a regular tetrahedron and&nbsp;the angle between them should be 109.5°. One hybrid orbital has paired electrons and it is nonbonding orbital. The other three orbitals are half-filled and they are bonding orbitals. But due to greater repulsion exerted by lone pair on bonding orbitals, the angle is reduced to 107°. Thus ammonia has distorted tetrahedral shape.</p>



<p>The three half-filled (containing unpaired electron) sp3 hybrid orbitals of nitrogen overlap axially with three half-filled 1s orbitals of three hydrogen atoms separately to form three covalent N-H bonds Hence geometry is tetrahedral pyramidal in which the nitrogen lies at the centre, three hydrogen atoms form the base and one pair of electrons forms the apex of the pyramid. H-N-H angle is 107°.</p>



<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Bonds:</strong></p>



<p>The three half-filled (containing unpaired electron) sp3 hybrid orbitals of nitrogen overlap axially with three half-filled 1s orbitals of three hydrogen atoms separately to form three covalent N-H bonds (sigma bonds). The fourth hybrid orbital containing lone pair of the electron remains non bonded. The bonds between Nitrogen and hydrogen are sp3- s. H – N – H bond angles are 107°. All N-H bonds in ammonia are of equal strength.</p>


<div class="wp-block-image">
<figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="553" height="142" src="https://thefactfactor.com/wp-content/uploads/2020/04/SP3-Hybridization-04.png" alt="Formation of Ammonia Molecule 03" class="wp-image-11014" srcset="https://thefactfactor.com/wp-content/uploads/2020/04/SP3-Hybridization-04.png 553w, https://thefactfactor.com/wp-content/uploads/2020/04/SP3-Hybridization-04-300x77.png 300w" sizes="auto, (max-width: 553px) 100vw, 553px" /></figure>
</div>


<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Type and Geometry:</strong></p>


<table border="1" align="center">
<tbody>
<tr>
<td width="182">
<p>Name of Molecule</p>
</td>
<td width="99">
<p>Ammonia</p>
</td>
</tr>
<tr>
<td width="182">
<p>Molecular Formula</p>
</td>
<td width="99">
<p>NH<sub>3</sub></p>
</td>
</tr>
<tr>
<td width="182">
<p>Type Of Hybridisation</p>
</td>
<td width="99">
<p>sp<sup>3</sup></p>
</td>
</tr>
<tr>
<td width="182">
<p>Geometry</p>
</td>
<td width="99">
<p>Pyramidal</p>
</td>
</tr>
<tr>
<td width="182">
<p>No. Of Bonds</p>
</td>
<td width="99">
<p>3</p>
</td>
</tr>
<tr>
<td width="182">
<p>No. Of Sigma bonds</p>
</td>
<td width="99">
<p>3 sigma</p>
</td>
</tr>
<tr>
<td width="182">
<p>Bond angle</p>
</td>
<td width="99">
<p>107°</p>
</td>
</tr>
<tr>
<td width="182">
<p>Overlaps</p>
</td>
<td width="99">
<p>3 sp<sup>3</sup> &#8211; s</p>
</td>
</tr>
<tr>
<td width="182">
<p>Bonds</p>
</td>
<td width="99">
<p>3 N-H</p>
</td>
</tr>
</tbody>
</table>


<p class="has-luminous-vivid-orange-color has-very-light-gray-background-color has-text-color has-background has-medium-font-size"><strong>Formation of Water Molecule:</strong></p>



<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Need of Hybridization:</strong></p>



<p>In oxygen atom there are two half-filled 2p orbitals and valency should be 2 and it is two.&nbsp; These three ‘p’ orbitals are perpendicular to each other and if they form bonds, the angle between them should be 90°.&nbsp; But the actual angle between bonding orbitals in water is 104.5°.&nbsp; To explain this variation the concept of hybridization is required.</p>



<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Electron Configuration:</strong></p>



<p>The atomic number of Oxygen is 8.&nbsp; Its configuration in ground state is 1s<sup>2</sup>, 2s<sup>2</sup>, 2p<sup>4</sup></p>


<div class="wp-block-image">
<figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="65" src="https://thefactfactor.com/wp-content/uploads/2020/04/SP3-Hybridization-05.png" alt="Formation of Water Molecule 01" class="wp-image-11016"/></figure>
</div>


<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Hybridization :</strong></p>



<p>In the formation of water molecule one 2s&nbsp;orbital and three 2p orbitals of Oxygen mix up forming four hybrid orbitals of equivalent energy. These four new equivalent orbitals are called sp<sup>3</sup> hybrid orbitals. They are identical in all respect. The two hybrid orbitals have paired electrons and they are non &#8211; bonding orbitals.&nbsp; Other two orbitals are half-filled and they are bonding orbitals. The nonbonding pairs of hybridized orbitals are called lone pairs. These hybridized orbitals are in the directions of four corners of a regular tetrahedron.</p>


<div class="wp-block-image">
<figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="59" src="https://thefactfactor.com/wp-content/uploads/2020/04/SP3-Hybridization-06.png" alt="Formation of Water Molecule 02" class="wp-image-11017"/></figure>
</div>


<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Angle and Geometry:</strong></p>



<p>Four sp3hybridised orbitals formed, repel each other and they should be directed towards the four corners of a regular tetrahedron and&nbsp;the angle between them should be 109.5°. But due to greater repulsion exerted by lone pair on bonding orbitals, the angle is reduced to 104.5<sup>0</sup>. Thus water has distorted the tetrahedral shape.</p>



<p>The two half-filled (containing unpaired electron) sp<sup>3</sup> hybrid orbitals of oxygen overlap axially with two half-filled 1s orbitals of two hydrogen atoms separately to form three O-H bonds. Thus geometry is angular or V-shaped, in which the oxygen lies at the centre, two hydrogen atoms occupy two corners of the tetrahedron and lone pair of electrons occupy remaining two corners of the tetrahedron. H-O-H angle is 104.5<sup>0</sup>.</p>



<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Bonds:</strong></p>



<p>The two half-filled (containing unpaired electron) sp3 hybrid orbitals of oxygen overlap axially with two half-filled 1s orbitals of two hydrogen atoms separately to form two O-H bonds (sigma bond).&nbsp; The remaining two hybrid orbitals containing a lone pair of the electron remains nonbonded.</p>


<div class="wp-block-image">
<figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="612" height="175" src="https://thefactfactor.com/wp-content/uploads/2020/04/SP3-Hybridization-07.png" alt="Formation of Water Molecule 03" class="wp-image-11018" srcset="https://thefactfactor.com/wp-content/uploads/2020/04/SP3-Hybridization-07.png 612w, https://thefactfactor.com/wp-content/uploads/2020/04/SP3-Hybridization-07-300x86.png 300w" sizes="auto, (max-width: 612px) 100vw, 612px" /></figure>
</div>


<p class="has-vivid-red-color has-text-color has-medium-font-size"><strong>Type and Geometry:</strong></p>


<table align="center" border="1">
<tbody>
<tr>
<td width="177">
<p>Name of Molecule</p>
</td>
<td width="171">
<p>Water</p>
</td>
</tr>
<tr>
<td width="177">
<p>Molecular Formula</p>
</td>
<td width="171">
<p>H<sub>2</sub>O</p>
</td>
</tr>
<tr>
<td width="177">
<p>Type Of Hybridisation</p>
</td>
<td width="171">
<p>sp<sup>3</sup></p>
</td>
</tr>
<tr>
<td width="177">
<p>Geometry</p>
</td>
<td width="171">
<p>Angular, V -shaped</p>
</td>
</tr>
<tr>
<td width="177">
<p>No. Of Bonds</p>
</td>
<td width="171">
<p>2</p>
</td>
</tr>
<tr>
<td width="177">
<p>No. Of Sigma bonds</p>
</td>
<td width="171">
<p>2 sigma</p>
</td>
</tr>
<tr>
<td width="177">
<p>Bond angle</p>
</td>
<td width="171">
<p>104.5°</p>
</td>
</tr>
<tr>
<td width="177">
<p>Overlaps</p>
</td>
<td width="171">
<p>2 sp<sup>3</sup> &#8211; s</p>
</td>
</tr>
<tr>
<td width="177">
<p>Bonds</p>
</td>
<td width="171">
<p>2 O-H</p>
</td>
</tr>
</tbody>
</table>


<h4 class="wp-block-heading"><strong>Science &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/" target="_blank">Chemistry</a> &gt; Physical Chemistry &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/nature-of-chemical-bond/" target="_blank">Nature of Chemical Bond</a> &gt; sp3 Hybridization</strong></h4>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/sp3-hybridization/11008/">sp3 Hybridization</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
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		<title>Hybridization of Orbitals</title>
		<link>https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/hybridization-of-orbitals/10990/</link>
					<comments>https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/hybridization-of-orbitals/10990/#comments</comments>
		
		<dc:creator><![CDATA[Hemant More]]></dc:creator>
		<pubDate>Tue, 31 Mar 2020 15:32:40 +0000</pubDate>
				<category><![CDATA[Physical Chemistry]]></category>
		<category><![CDATA[Axial overlap]]></category>
		<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[Covalent bond]]></category>
		<category><![CDATA[Excited state]]></category>
		<category><![CDATA[Formation of Ammonia molecule]]></category>
		<category><![CDATA[Formation of Methane molecule]]></category>
		<category><![CDATA[Formation of water molecule]]></category>
		<category><![CDATA[Geometry of molecule]]></category>
		<category><![CDATA[Ground state]]></category>
		<category><![CDATA[Hybridisation]]></category>
		<category><![CDATA[Hybridization]]></category>
		<category><![CDATA[Hybridized orbitals]]></category>
		<category><![CDATA[Hybridized state]]></category>
		<category><![CDATA[Lateral overlap]]></category>
		<category><![CDATA[Nature of chemical bond]]></category>
		<category><![CDATA[Overlapping of orbitals]]></category>
		<category><![CDATA[P-P overlap]]></category>
		<category><![CDATA[pi bond]]></category>
		<category><![CDATA[S-P overlap]]></category>
		<category><![CDATA[S-S overlap]]></category>
		<category><![CDATA[sigma bond]]></category>
		<category><![CDATA[SP hybridization]]></category>
		<category><![CDATA[SP2 hybridization]]></category>
		<category><![CDATA[SP3 hybridization]]></category>
		<category><![CDATA[Tetrahedral geometry]]></category>
		<category><![CDATA[Valence bond theory]]></category>
		<guid isPermaLink="false">https://thefactfactor.com/?p=10990</guid>

					<description><![CDATA[<p>Science &#62; Chemistry &#62; Physical Chemistry &#62; Nature of Chemical Bond &#62; Hybridization of Orbitals In this article, we shall study the concept of hybridization of orbitals. This concept overcomes the limitations of valence bond theory. Need for Hybridization Concept: A simple approach based on the overlap of s and p orbitals can be applied [&#8230;]</p>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/hybridization-of-orbitals/10990/">Hybridization of Orbitals</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
]]></description>
										<content:encoded><![CDATA[
<h4 class="wp-block-heading"><strong>Science &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/" target="_blank">Chemistry</a> &gt; Physical Chemistry &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/nature-of-chemical-bond/" target="_blank">Nature of Chemical Bond</a> &gt; Hybridization of Orbitals</strong></h4>



<p>In this article, we shall study the concept of hybridization of orbitals. This concept overcomes the limitations of valence bond theory. </p>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Need for Hybridization Concept:</strong></p>



<p>A simple approach based on the overlap of s and p orbitals can be applied to many molecules, but it fails to explain the formation of compounds of Beryllium (Be), Boron (B), and carbon (C). The electronic configurations of Be, B, and C in the ground state are as follows.</p>



<p>The atoms of Beryllium Be (Z = 4) &nbsp;Electronic configuration is 1s<sup>2</sup> 2s<sup>2</sup> (With no unpaired electrons).</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="55" src="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-01.png" alt="Hybridization 01 Beryllium" class="wp-image-10997"/></figure></div>



<p>The atom of Boron B (Z = 5) &nbsp; Electronic configuration is 1s<sup>2</sup> 2s<sup>2</sup> 2p<sup>1</sup> (With one unpaired electron).</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="55" src="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-02.png" alt="Hybridization 02 Boron" class="wp-image-10998"/></figure></div>



<p>The atom of Carbon C (Z = 6) &nbsp; Electronic configuration is 1s<sup>2</sup> 2s<sup>2</sup> 2p<sup>2</sup> (With two unpaired electrons).</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="45" src="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-03.png" alt="Hybridization 03 Carbon" class="wp-image-10999"/></figure></div>



<p>According to
valence bond theory valency of an element depends on a number of unpaired
electrons in the orbitals. Thus Beryllium, Boron, and Carbon should be
zero-valent, monovalent and divalent respectively.&nbsp; However, these
elements form the compounds having valency 2, 3, and 4 respectively. Valence
bond theory fails to explain this phenomenon. This is explained by hybridization.</p>



<p>Valence Bond Theory fails to explain the observed geometry of the molecules of water and ammonia e.g. in the formation of H<sub>2</sub>O molecule, the H – O – H bond angle should be 90°. But the measured bond angle is 104.3° and the molecule is V-Shaped. Valence bond theory failed to explain this change. To explain The equivalence of bonds we have to use the concept of a process of mixing and recasting of atomic orbitals. For e.g. all the four C-H bonds in methane molecule are equivalent in terms of strength, energy, etc. It can be explained on the basis of hybridization.</p>



<p>Note: The above paragraphs give limitations of the valence bond theory.</p>



<p class="has-text-color has-background has-medium-font-size has-luminous-vivid-orange-color has-very-light-gray-background-color"><strong>Hybridization: </strong></p>



<p>Mixing and recasting or orbitals of an atom (same atom) with nearly equal energy to form new equivalent orbitals with maximum symmetry and definite orientation in space is called hybridization.</p>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Steps Involved in Hybridization:</strong></p>



<h4 class="wp-block-heading"><strong>Step -1: Formation of excited state:</strong></h4>



<p>The atom in the ground state takes up some energy and goes to the excited state.&nbsp; In this process, usually, a pair of electrons in lower energy orbital is split up and one of the electron from this pair is transferred to some empty slightly higher but almost equal energy orbital.&nbsp; Thus the excited state has a larger number of half-filled orbitals. This new number of half-filled orbitals decides the number of covalent bonds an atom can form.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="150" src="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-04.png" alt="" class="wp-image-11000"/></figure></div>



<h4 class="wp-block-heading"><strong>Step = 2: Mixing and recasting of atomic orbitals:</strong></h4>



<p>The orbitals of nearly the same energy in an excited state now hybridize i.e. unite and redistribute themselves giving hybrid orbitals of the same energy and definite orientation in space. Mixing and recasting or orbitals of an atom(same atom) with nearly equal energy to form new equivalent orbitals with maximum symmetry and definite orientation in space is called hybridization.</p>



<p>One 2-s
orbital and three p- orbitals mix together and recast themselves to form new
four sp<sup>3</sup> hybridized orbitals.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="325" height="105" src="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-05.png" alt="" class="wp-image-11001" srcset="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-05.png 325w, https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-05-300x97.png 300w" sizes="auto, (max-width: 325px) 100vw, 325px" /></figure></div>



<h4 class="wp-block-heading"><strong>Step
&#8211; 3: Proper Orientation of the Hybrid Orbitals in Space:</strong></h4>



<p>The hybrid orbitals then get arranged in space in such a way to minimize mutual repulsion. Each hybrid orbital is more concentrated on one side of the nucleus. Due to this greater overlap is achieved and a stronger bond is formed.</p>



<p>Thus in
carbon, the four hybrid sp3&nbsp;orbitals arrange themselves at four corners of
a tetrahedron to minimize mutual repulsion.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="542" height="150" src="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-06.png" alt="" class="wp-image-11002" srcset="https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-06.png 542w, https://thefactfactor.com/wp-content/uploads/2020/03/Hybridization-of-Orbitals-06-300x83.png 300w" sizes="auto, (max-width: 542px) 100vw, 542px" /></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Essential Condition for Hybridization:</strong></p>



<p>The orbitals
participating in hybridization should have nearly the same energy. Thus in the
formation of methane, the 2s and 2p orbitals of carbon have nearly the same
energies, so that the recasting of orbitals is possible.&nbsp; But
hybridization of 2s and 3p is not possible because there is much difference between
their energies.</p>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Characteristics or Rules of hybridization:</strong></p>



<ul class="wp-block-list"><li>Atomic orbitals undergoing hybridization should belong to the same atom or ion.</li><li>Atomic orbitals participating in hybridization should have nearly the same energy. Thus 2s and 2p can hybridize, 3s and 3p can also hybridize, but 2s and 3p cannot.</li><li>The total number of hybrid orbitals formed is equal to the number of atomic orbitals involved in the hybridization process.</li><li>All hybrid orbitals are identical with respect to energy and directional character.</li><li>The hybrid orbitals may differ from one other in their orientations.</li><li>The shape of the hybrid orbitals is different from that of the original atomic orbital.</li><li>Similar to atomic orbitals, each hybrid orbital can have a maximum of two electrons.</li><li>The hybrid orbitals are concentrated in one particular direction to achieve greater overlapping.</li><li>The hybrid orbitals have maximum symmetry and definite orientation in space so that the mutual force of repulsion of electrons is avoided.</li></ul>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Types of Hybridization and Geometry of Molecules:</strong></p>



<p>The hybridization involving s and p orbitals are of the following three types: </p>



<ul class="wp-block-list"><li>Tetrahedral or sp<sup>3&nbsp;</sup>hybridization e.g. CH<sub>4</sub>, NH<sub>3</sub>, H<sub>2</sub>O</li><li>Trigonal or sp<sup>2</sup> e.g. BF<sub>3</sub>, C<sub>2</sub>H<sub>4</sub>.</li><li>Diagonal or sp hybridization e.g. BeF<sub>2</sub>, C<sub>2</sub>H<sub>2</sub></li></ul>



<p>Their names indicate the orientation of the orbitals in space and the designation (sp<sup>2</sup>, sp<sup>3</sup>, etc) indicates the number and types of atomic orbitals involved in hybridization.</p>



<h4 class="wp-block-heading"><strong>Science &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/" target="_blank">Chemistry</a> &gt; Physical Chemistry &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/nature-of-chemical-bond/" target="_blank">Nature of Chemical Bond</a> &gt; Hybridization of Orbitals</strong></h4>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/hybridization-of-orbitals/10990/">Hybridization of Orbitals</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
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		<item>
		<title>Formation of Covalent Bonds</title>
		<link>https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/covalent-bond/10926/</link>
					<comments>https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/covalent-bond/10926/#respond</comments>
		
		<dc:creator><![CDATA[Hemant More]]></dc:creator>
		<pubDate>Tue, 31 Mar 2020 12:25:32 +0000</pubDate>
				<category><![CDATA[Physical Chemistry]]></category>
		<category><![CDATA[Atomic number]]></category>
		<category><![CDATA[Bond]]></category>
		<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[Coordinate bond]]></category>
		<category><![CDATA[Covalent bond]]></category>
		<category><![CDATA[Dash formula]]></category>
		<category><![CDATA[dash structure]]></category>
		<category><![CDATA[Dot formula]]></category>
		<category><![CDATA[Dot structure]]></category>
		<category><![CDATA[Duplet]]></category>
		<category><![CDATA[Electron pair bonds]]></category>
		<category><![CDATA[Electronic configuration]]></category>
		<category><![CDATA[Electrovalent bond]]></category>
		<category><![CDATA[Expanded octet]]></category>
		<category><![CDATA[Formation of Acetylene molecule]]></category>
		<category><![CDATA[Formation of Ammonia molecule]]></category>
		<category><![CDATA[Formation of chlorine molecule]]></category>
		<category><![CDATA[Formation of Ethane molecule]]></category>
		<category><![CDATA[Formation of Ethylene molecule]]></category>
		<category><![CDATA[Formation of hydrogen chloride molecule]]></category>
		<category><![CDATA[Formation of Hydrogen molecule]]></category>
		<category><![CDATA[Formation of Methane molecule]]></category>
		<category><![CDATA[Formation of nitrogen molecule]]></category>
		<category><![CDATA[Formation of oxygen molecule]]></category>
		<category><![CDATA[Formation of water molecule]]></category>
		<category><![CDATA[Geometry of molecule]]></category>
		<category><![CDATA[Incomplete octet]]></category>
		<category><![CDATA[Ionic bond]]></category>
		<category><![CDATA[Lewis structure]]></category>
		<category><![CDATA[Nature of chemical bond]]></category>
		<category><![CDATA[Octet]]></category>
		<category><![CDATA[Octet theory]]></category>
		<category><![CDATA[Valence electrons]]></category>
		<category><![CDATA[Valency orbit]]></category>
		<guid isPermaLink="false">https://thefactfactor.com/?p=10926</guid>

					<description><![CDATA[<p>Science &#62; Chemistry &#62; Physical Chemistry &#62; Nature of Chemical Bond &#62; Formation of Covalent Bonds In previous articles, we have seen formation of ionic bonds. In this article, we shall study the concept of the formation of a covalent bond. Covalent Bonds or&#160;Electron Pair Bonds: A bond established between two identical or different atoms [&#8230;]</p>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/covalent-bond/10926/">Formation of Covalent Bonds</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
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<h4 class="wp-block-heading"><strong>Science &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/" target="_blank">Chemistry</a> &gt; Physical Chemistry &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/nature-of-chemical-bond/" target="_blank">Nature of Chemical Bond</a> &gt; Formation of Covalent Bonds</strong></h4>



<p>In previous articles, we have seen formation of ionic bonds. In this article, we shall study the concept of the formation of a covalent bond.</p>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Covalent Bonds or&nbsp;Electron Pair Bonds:</strong></p>



<p>A bond established between two identical or different atoms by sharing one or more pairs of electrons is known as a covalent bond. The attractive force which comes into existence due to the mutual sharing of electrons between two atoms having similar electronegativity or having a small difference in electronegativities is called a covalent bond.</p>



<p>No ionic
bond is possible between two atoms having similar electronegativities. Hence to
explain the bonding between such atoms Lewis introduced the concept of covalent
bonds.</p>



<p>Each atom contributes one electron to form a common pair i.e. equal contribution of electrons followed by equal sharing. If one electron pair is shared, it is known as a single covalent bond.&nbsp; If two electron pairs are shared, it is a double covalent bond and so on. In CI2, O2, CH4, H2O, etc. there are covalent bonds.</p>



<p class="has-text-color has-background has-medium-font-size has-luminous-vivid-orange-color has-very-light-gray-background-color"><strong>Examples of Covalent Bonds:</strong></p>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Hydrogen Molecule:</strong></p>



<p>Electronic configuration of hydrogen H (Z = 1) is (1) Hydrogen has one electron in its valence shell. It tries&nbsp;to acquire a stable configuration (2) by sharing its one electron with another hydrogen atom.</p>



<p>When two
hydrogen atoms approach each other, at a certain distance between the nuclei,
they share their valence electrons and form a shared pair of electrons. The
shared pair belongs to each atom equally. As only one pair is shared between
the two hydrogen atoms, they are joined to each other by a single covalent
bond.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="396" height="128" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-01.png" alt="covalent bond" class="wp-image-10933" srcset="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-01.png 396w, https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-01-300x97.png 300w" sizes="auto, (max-width: 396px) 100vw, 396px" /></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Chlorine Molecule:</strong></p>



<p>Electronic configuration of chlorine Cl (Z = 17) is (2, 8, 7). Chlorine has 7 electrons in its valence shell.&nbsp;It can acquire a stable configuration (2, 8, 8) of the nearest inert gas (Ar) by sharing&nbsp;one electron with another chlorine atom.</p>



<p>When two chlorine atoms approach each other, at a certain distance between the nuclei, they share their valence electrons and form a shared pair of electrons. The shared pair belongs to each atom equally. As only one pair is shared between the two chlorine atoms, they are joined to each other by a single covalent bond.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="437" height="137" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-02.png" alt="covalent bond" class="wp-image-10934" srcset="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-02.png 437w, https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-02-300x94.png 300w" sizes="auto, (max-width: 437px) 100vw, 437px" /></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Hydrogen Chloride Molecule:</strong></p>



<p>Electronic configuration of hydrogen H (Z = 1) is&nbsp; (1) &nbsp;Hydrogen has one electron in its valence shell. It tries&nbsp;to acquire a stable configuration (2) by sharing its one electron with the chlorine atom.&nbsp;Electronic configuration of chlorine Cl (Z = 17) is (2, 8, 7). Chlorine has 7 electrons in its valence shell.&nbsp;It can acquire a stable configuration (2, 8, 8) of nearest inert gas (Ar) by sharing&nbsp;one electron with the hydrogen atom.</p>



<p>When hydrogen and chlorine atoms approach each other, at a certain distance between the nuclei, they share their valence electrons and form a shared pair of electrons. The shared pair belongs to each atom equally. As only one pair is shared between the hydrogen and chlorine atoms, they are joined to each other by a single covalent bond.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="412" height="188" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-04.png" alt="covalent bond" class="wp-image-10936" srcset="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-04.png 412w, https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-04-300x137.png 300w" sizes="auto, (max-width: 412px) 100vw, 412px" /></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Ammonia Molecule:</strong></p>



<p>Electronic
configuration of nitrogen N (Z = 7) is (2, 5). Nitrogen has 5 electrons in its
valence shell.&nbsp;It can acquire stable configuration (2, 8) of nearest inert
gas (Ne) by sharing&nbsp;one electron each with three hydrogen atom.</p>



<p>When three hydrogen atoms approach nitrogen atom, at a certain distance between the nuclei, it shares one valence electron each with the nitrogen atom and forms three shared pairs of electrons with three hydrogen atoms. The shared pair belongs to each atom equally. As only one pair is shared between the atoms, they are joined to each other by a single covalent bond.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="460" height="204" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-05.png" alt="covalent bond" class="wp-image-10937" srcset="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-05.png 460w, https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-05-300x133.png 300w" sizes="auto, (max-width: 460px) 100vw, 460px" /></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Water Molecule:</strong></p>



<p>Electronic
configuration of oxygen O (Z = 8) is (2, 6). Oxygen has 6 electrons in its
valence shell.&nbsp;It can acquire stable configuration (2, 8) of nearest inert
gas (Ne) by sharing&nbsp;one electron each with two hydrogen atom.</p>



<p>When two hydrogen atoms approach oxygen atom, at a certain distance between the nuclei, it shares one valence electron each with two hydrogen atoms and forms two shared pairs of electrons with two hydrogen atoms. The shared pair belongs to each atom equally. As only one pair is shared between the atoms, they are joined to each other by a single covalent bond.</p>



<div class="wp-block-image"><figure class="aligncenter size-large is-resized"><img loading="lazy" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-06.png" alt="covalent bond" class="wp-image-10938" width="288" height="116" srcset="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-06.png 379w, https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-06-300x121.png 300w" sizes="auto, (max-width: 288px) 100vw, 288px" /></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Phosphorous Trichloride Molecule:</strong></p>



<p>Electronic configuration of phosphorous P (Z = 15) is (2, 8, 5). Phosphorous has 5 electrons in its valence shell.&nbsp;It can acquire stable configuration (2, 8, 8) of nearest inert gas (Ar) by sharing&nbsp;one electron each with three chlorine atoms.&nbsp;Electronic configuration of chlorine Cl (Z = 17) is (2, 8, 7). Chlorine has 7 electrons in its valence shell.&nbsp;It can acquire a stable configuration (2, 8, 8) of the nearest inert gas (Ar) by sharing&nbsp;one electron with another atom.</p>



<p>When three chlorine atoms approach phosphorous atom, at a certain distance between the nuclei, it shares one valence electron each with the three chlorine atoms and forms three shared pairs of electrons with three chlorine atoms. The shared pair belongs to each atom equally. As only one pair is shared between the atoms, they are joined to each other by a single covalent bond.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="90" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-07.png" alt="covalent bond" class="wp-image-10939"/></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Methane Molecule:</strong></p>



<p>Electronic
configuration of carbon C (Z = 6) is (2, 4). Carbon has 4 electrons in its
valence shell.&nbsp;It can acquire stable configuration (2, 8) of nearest inert
gas (Ne) by sharing&nbsp;one electron each with four hydrogen atoms.</p>



<p>When four hydrogen atoms approach phosphorous atom, at a certain distance between the nuclei, it shares one valence electron each with the four hydrogen atoms and forms four shared pairs of electrons with four hydrogen atoms. The shared pair belongs to each atom equally. As only one pair is shared between the atoms, they are joined to each other by a single covalent bond.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="170" height="77" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-08.png" alt="covalent bond" class="wp-image-10940"/></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Ethane Molecule:</strong></p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="93" height="73" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-09.png" alt="" class="wp-image-10941"/></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Oxygen Molecule:</strong></p>



<p>Consider the formation of the oxygen molecule.&nbsp;Electronic configuration of oxygen O (Z = 8) is (2, 6). Oxygen has 6 electrons in its valence shell.&nbsp;It can acquire a stable configuration (2, 8) of nearest inert gas (Ne) by sharing two electrons with another oxygen atom. The two atoms share two pairs of electrons between them completing octet of each. two shared pairs constitute a double bond.</p>



<p class="has-text-align-center">O&nbsp; &nbsp; &nbsp; &nbsp; +&nbsp; &nbsp; &nbsp; O&nbsp;
&nbsp; &nbsp; &nbsp; →&nbsp; &nbsp;O=O</p>



<p class="has-text-align-center">(2,6)&nbsp; &nbsp; &nbsp; (2,6)&nbsp; &nbsp; &nbsp;
&nbsp;(2,8) (2,8)</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="230" height="36" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-10.png" alt="" class="wp-image-10942"/></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Nitrogen Molecule:</strong></p>



<p>Consider the formation of the nitrogen molecule.&nbsp;Electronic configuration of nitrogen (Z = 7) is (2, 5). Nitrogen has 5 electrons in its valence shell.&nbsp;It can acquire a stable configuration (2, 8) of nearest inert gas (Ne) by sharing three electrons with another nitrogen atom. The two atoms share three pairs of electrons between them completing octet of each. Three shared pairs constitute a triple bond.</p>



<p class="has-text-align-center">&nbsp;N&nbsp; &nbsp; &nbsp; &nbsp; +&nbsp; &nbsp; &nbsp;
N&nbsp; &nbsp; &nbsp; &nbsp; →&nbsp; &nbsp;N≡N</p>



<p class="has-text-align-center">(2,5)&nbsp; &nbsp; &nbsp; (2,5)&nbsp; &nbsp; &nbsp;
&nbsp;(2,8) (2,8)</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="360" height="42" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-11.png" alt="Covalent Bond" class="wp-image-10943" srcset="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-11.png 360w, https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-11-300x35.png 300w" sizes="auto, (max-width: 360px) 100vw, 360px" /></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Ethene (Ethylene) Molecule:</strong></p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="93" height="62" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-12.png" alt="" class="wp-image-10944"/></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Formation of Ethyne (Acetylene) Molecule:</strong></p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="102" height="39" src="https://thefactfactor.com/wp-content/uploads/2020/03/Covaent-Bond-13.png" alt="" class="wp-image-10945"/></figure></div>



<h4 class="wp-block-heading"><strong>Science &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/" target="_blank">Chemistry</a> &gt; Physical Chemistry &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/nature-of-chemical-bond/" target="_blank">Nature of Chemical Bond</a> &gt; Formation of Covalent Bonds</strong></h4>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/physical-chemistry/covalent-bond/10926/">Formation of Covalent Bonds</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
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