Eclipsed conformation

<h2 id="organic-chemistry">Organic chemistry</h2>
Conformations can be described by <a href="/facts/Dihedral_angles/C9WEJsuS">dihedral angles</a>, which are used to determine the placements of atoms and their distance from one another and can be visualized by <a href="/facts/Newman_projection/byBFKtuC">Newman projections</a>. A dihedral angle can indicate <a href="/facts/Staggered_conformation/EYoNI8Pv">staggered</a> and eclipsed orientation, but is specifically used to determine the angle between two specific atoms on opposing carbons. Different conformations have unequal energies, creating an <a href="/facts/Energy_barrier/GqkgPvo0">energy barrier</a> to bond rotation which is known as <a href="/facts/Strain_(chemistry)/xhAQQMH8">torsional strain</a>. In particular, eclipsed conformations tend to have raised energies due to the repulsion of the electron clouds of the eclipsed substituents. The relative energies of different conformations can be visualized using graphs. In the example of <a href="/facts/Ethane/BGCzc6yh">ethane</a>, such a graph shows that rotation around the carbon-carbon bond is not entirely free but that an energy barrier exists. The ethane molecule in the eclipsed conformation is said to suffer from torsional strain, and by a rotation around the carbon carbon bond to the staggered conformation around 12.5 kJ/mol of <a href="/facts/Alkane_stereochemistry/EYd5Kyvl">torsional energy</a> is released. In the case of <a href="/facts/Butane/InIHpYlY">butane</a> and its four-carbon chain, three carbon-carbon bonds are available to rotate. The example below is looking down the C2 and C3 bond. Below is the sawhorse and Newman representation of butane in an eclipsed conformation with the two CH3 groups (C1 and C4) at a 0-degree angle from one another (left).
If the front is rotated 60° clockwise, the butane molecule is now in a staggered conformation (right). This conformation is more specifically referred to as the <a href="/facts/Gauche_conformation/JflrT5Ws">gauche conformation</a> of butane. This is due to the fact that the methyl groups are staggered, but only 60° from one another. This conformation is more energetically favored than the eclipsed conformation, but it is not the most energetically favorable conformation. Another 60° rotation gives us a second eclipsed conformation where both methyl groups are aligned with hydrogen atoms. One more 60 rotation produces another staggered conformation referred to as the <a href="/facts/Anti_conformation/EYd5Kyvl">anti conformation</a>. This occurs when the methyl groups are positioned opposite (180°) of one another. This is the most energetically favorable conformation. <a class="footnote-ref" id="fnref:3" href="#fn:3">3</a>
The minima can be seen on the graph at 60, 180 and 300 degrees while the maxima can bee see at 0, 120, 240, and 360 degrees. The maxima represent the eclipsed conformations due to the dihedral angle of zero degrees.<a class="footnote-ref" id="fnref:4" href="#fn:4">4</a>

<h2 id="structural-applications">Structural applications</h2>
As established by <a href="/facts/X-ray_crystallography/WtI0F5DN">X-ray crystallography</a>, <a href="/facts/Potassium_octachlorodimolybdate/FaD7XD7p">octachlorodimolybdate(II)</a> anion ([Mo2Cl8]4-) has an eclipsed conformation. This sterically unfavorable geometry is given as evidence for a <a href="/facts/Quadruple_bond/hxpcR3o2">quadruple bond</a> between the Mo centers.<a class="footnote-ref" id="fnref:5" href="#fn:5">5</a>
Experiments such as X-ray and <a href="/facts/Electron_diffraction/IlFzQyVu">electron diffraction analyses</a>, <a href="/facts/Nuclear_magnetic_resonance_spectroscopy/SFKgdthI">nuclear magnetic resonance</a>, <a href="/facts/Microwave_spectroscopy/kfc6kCh8">microwave spectroscopies</a>, and more have allowed researchers to determine which cycloalkane structures are the most stable based on the different possible conformations. Another method that was shown successful is <a href="/facts/Molecular_mechanics/6wPpARWP">molecular mechanics</a>, a <a href="/facts/Computational_chemistry/KyuCgRV3">computational method</a> that allows the total strain energies of different conformations to be found and analyzed. It was found that the most stable conformations had lower energies based on values of energy due to bond distances and bond angles.<a class="footnote-ref" id="fnref:6" href="#fn:6">6</a>

In many cases, isomers of alkanes with branched chains have lower boiling points than those that are unbranched, which has been shown through experimentation with isomers of C8H18. This is because of a combination of intermolecular forces and size that results from the branched chains. The more branches that an alkane has, the more extended its shape is; meanwhile, if it is less branched then it will have more intermolecular attractive forces that will need to be broken which is the cause of the increased boiling point for unbranched alkanes. In another case, <a href="/facts/2%2c2%2c3%2c3-tetramethylbutane/r8aKmCwg">2,2,3,3-tetramethylbutane</a> is shaped more like an ellipsoid causing it to be able to form a crystal lattice which raises the melting point of the molecule because it will take more energy to transition from a solid to a liquid state.<a class="footnote-ref" id="fnref:7" href="#fn:7">7</a>
<h2 id="see-also">See also</h2>
<ul><li><a href="/facts/Gauche_effect/fzCRmMKb">Gauche effect</a></li></ul>

<h2 id="references">References</h2>

<ol>
<li id="fn:1">Eliel, Ernest L.; Wilen, Samuel H. (1994). Stereochemistry of Organic Compounds. Wiley. p. 1197. ISBN 978-0-471-01670-0. <a href="978-0-471-01670-0" target="_blank">978-0-471-01670-0</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></li>
<li id="fn:2">Ashenhurst, James (February 28, 2020). "Staggered vs Eclipsed Conformations of Ethane". Mastering Organic Chemistry. Retrieved November 15, 2022. <a href="https://www.masterorganicchemistry.com/2020/02/28/staggered-vs-eclipsed-conformations-of-ethane/" target="_blank">https://www.masterorganicchemistry.com/2020/02/28/staggered-vs-eclipsed-conformations-of-ethane/</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></li>
<li id="fn:3">"hydrocarbon - Three-dimensional structures | Britannica". www.britannica.com. Retrieved 2022-11-15. <a href="https://www.britannica.com/science/hydrocarbon/Three-dimensional-structures" target="_blank">https://www.britannica.com/science/hydrocarbon/Three-dimensional-structures</a> <a href="#fnref:3" class="footnote-back-ref">↩</a></li>
<li id="fn:4">"3.4.1. Newman Projections". Chemistry LibreTexts. 2015-06-16. Retrieved 2022-11-15. <a href="https://chem.libretexts.org/Courses/Purdue/Purdue_Chem_26100%3A_Organic_Chemistry_I_(Wenthold)/Chapter_03%3A_Structure_of_Alkanes/3.4.%09Structure_and_Conformations_of_Alkanes/3.4.1._Newman_Projections" target="_blank">https://chem.libretexts.org/Courses/Purdue/Purdue_Chem_26100%3A_Organic_Chemistry_I_(Wenthold)/Chapter_03%3A_Structure_of_Alkanes/3.4.%09Structure_and_Conformations_of_Alkanes/3.4.1._Newman_Projections</a> <a href="#fnref:4" class="footnote-back-ref">↩</a></li>
<li id="fn:5">Brignole, A. B.; Cotton, F. A.; Dori, Z. (1972). Rhenium and Molybdenum Compounds Containing Quadruple Bonds. Vol. 13. pp. 81–89. doi:10.1002/9780470132449.ch15. ISBN 978-0-470-13244-9. {{cite book}}: |journal= ignored (help) <a href="978-0-470-13244-9" target="_blank">978-0-470-13244-9</a> <a href="#fnref:5" class="footnote-back-ref">↩</a></li>
<li id="fn:6">"hydrocarbon - Three-Dimensional Structures". Britannica. Retrieved November 15, 2022. <a href="https://www.britannica.com/science/hydrocarbon/Three-dimensional-structures" target="_blank">https://www.britannica.com/science/hydrocarbon/Three-dimensional-structures</a> <a href="#fnref:6" class="footnote-back-ref">↩</a></li>
<li id="fn:7">"hydrocarbon - Three-Dimensional Structures". Britannica. Retrieved November 15, 2022. <a href="https://www.britannica.com/science/hydrocarbon/Three-dimensional-structures" target="_blank">https://www.britannica.com/science/hydrocarbon/Three-dimensional-structures</a> <a href="#fnref:7" class="footnote-back-ref">↩</a></li>
</ol>

Eclipsed conformation open-in-new

Eclipsed conformation