{"id":205522,"date":"2025-03-24T17:30:12","date_gmt":"2025-03-24T17:30:12","guid":{"rendered":"https:\/\/learnexams.com\/blog\/?p=205522"},"modified":"2025-03-24T17:30:14","modified_gmt":"2025-03-24T17:30:14","slug":"the-most-stable-conformation-of-cis-1-tert-butyl-2-mothylcyclohexane-is-the-one-in-which","status":"publish","type":"post","link":"https:\/\/www.learnexams.com\/blog\/2025\/03\/24\/the-most-stable-conformation-of-cis-1-tert-butyl-2-mothylcyclohexane-is-the-one-in-which\/","title":{"rendered":"The Most Stable Conformation Of Cis-1-Tert-Butyl-2-Mothylcyclohexane Is The One In Which"},"content":{"rendered":"\n<p>The Most Stable Conformation Of Cis-1-Tert-Butyl-2-Mothylcyclohexane Is The One In Which:<\/p>\n\n\n\n<p>A) The Tert -Butyl Group Is Axial And The Methyl Group In Equatorial.<br>B) The Methyl Group Is Axial And The Tert -Butyl Group Is Equatorial.<br>C) Both Groups Are Axial.<br>D) Both Groups Are Equatorial.<br>E) None Of The Above<\/p>\n\n\n\n<p><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-ast-global-color-6-color\"><strong>The correct answer and explanation is :<\/strong><\/mark><\/p>\n\n\n\n<p>The correct answer is <strong>B) The Methyl Group Is Axial And The Tert-Butyl Group Is Equatorial<\/strong>.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Explanation:<\/h3>\n\n\n\n<p>To determine the most stable conformation of <strong>cis-1-tert-butyl-2-methylcyclohexane<\/strong>, we need to consider the following factors:<\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li><strong>Steric Hindrance and Size of Groups:<\/strong><\/li>\n<\/ol>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Tert-butyl group (C\u2084H\u2089)<\/strong> is bulky and will experience significant steric strain if placed in the <strong>axial<\/strong> position. This is because axial positions in cyclohexane conformations are in close proximity to the other axial substituents on the same side of the ring (called <strong>1,3-diaxial interactions<\/strong>). These interactions cause steric hindrance and lead to increased strain when a large group occupies the axial position.<\/li>\n\n\n\n<li><strong>Methyl group (CH\u2083)<\/strong> is smaller and can more easily be accommodated in the <strong>axial<\/strong> position because it doesn&#8217;t introduce as much steric strain compared to the tert-butyl group.<\/li>\n<\/ul>\n\n\n\n<ol class=\"wp-block-list\">\n<li><strong>Conformation of Cyclohexane Rings:<\/strong><\/li>\n<\/ol>\n\n\n\n<ul class=\"wp-block-list\">\n<li>The chair conformation of cyclohexane allows for substituents to occupy either axial or equatorial positions.<\/li>\n\n\n\n<li>The <strong>equatorial position<\/strong> is generally more favorable for large substituents, such as the <strong>tert-butyl group<\/strong>, because it minimizes steric interactions.<\/li>\n\n\n\n<li>The <strong>axial position<\/strong> is typically preferred for smaller substituents, like the <strong>methyl group<\/strong>, to avoid steric clashes.<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Most Stable Conformation:<\/h3>\n\n\n\n<p>In the <strong>cis<\/strong> form of 1-tert-butyl-2-methylcyclohexane:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>The <strong>tert-butyl group<\/strong> will prefer to be <strong>equatorial<\/strong> because it is large and its axial positioning would create significant steric hindrance (1,3-diaxial interactions).<\/li>\n\n\n\n<li>The <strong>methyl group<\/strong> will prefer to be <strong>axial<\/strong> since it is smaller and can fit better in this position with less steric interference.<\/li>\n<\/ul>\n\n\n\n<p>Thus, the most stable conformation is one where the <strong>tert-butyl group is equatorial<\/strong>, and the <strong>methyl group is axial<\/strong>.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Image:<\/h3>\n\n\n\n<p>Here\u2019s a diagram of the two possible chair conformations of <strong>cis-1-tert-butyl-2-methylcyclohexane<\/strong>, showing the most stable conformation (with tert-butyl equatorial and methyl axial).<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" src=\"https:\/\/learnexams.com\/blog\/wp-content\/uploads\/2025\/03\/image-1332.png\" alt=\"\" class=\"wp-image-205523\"\/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>The Most Stable Conformation Of Cis-1-Tert-Butyl-2-Mothylcyclohexane Is The One In Which: A) The Tert -Butyl Group Is Axial And The Methyl Group In Equatorial.B) The Methyl Group Is Axial And The Tert -Butyl Group Is Equatorial.C) Both Groups Are Axial.D) Both Groups Are Equatorial.E) None Of The Above The correct answer and explanation is : [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center 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