{"id":222024,"date":"2025-05-30T19:56:27","date_gmt":"2025-05-30T19:56:27","guid":{"rendered":"https:\/\/learnexams.com\/blog\/?p=222024"},"modified":"2025-05-30T19:56:29","modified_gmt":"2025-05-30T19:56:29","slug":"the-specific-rotation-of-carvone-is-61-degrees-while-the-specific-rotation-of-r-carvone-is-61-degrees","status":"publish","type":"post","link":"https:\/\/www.learnexams.com\/blog\/2025\/05\/30\/the-specific-rotation-of-carvone-is-61-degrees-while-the-specific-rotation-of-r-carvone-is-61-degrees\/","title":{"rendered":"The specific rotation of -Carvone is +61 degrees, while the specific rotation of (R)-Carvone is -61 degrees"},"content":{"rendered":"\n<p>The specific rotation of -Carvone is +61 degrees, while the specific rotation of (R)-Carvone is -61 degrees. If a sample of mixture of the two enantiomers has a specific rotation of -40.58 degrees<\/p>\n\n\n\n<p>Part I. What is the percent enantiomeric excess of the mixture?<br>a) +24.75<br>b) -24.75<br>c) 24.75<br>d) -66.52<br>e) 66.52<\/p>\n\n\n\n<p>Part II. What is the percentage of each enantiomer in the above mixture?<br>a) of and of S<br>b) of and of<br>c) of and of<br>d) racemic mixture of and<br>e) of and of<\/p>\n\n\n\n<p><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-ast-global-color-0-color\">The Correct Answer and Explanation is:<\/mark><\/strong><\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><strong>Part I: What is the percent enantiomeric excess (ee)?<\/strong><\/h3>\n\n\n\n<p>We are given:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Specific rotation of pure <strong>(S)-Carvone<\/strong>: <strong>+61\u00b0<\/strong><\/li>\n\n\n\n<li>Specific rotation of pure <strong>(R)-Carvone<\/strong>: <strong>\u201361\u00b0<\/strong><\/li>\n\n\n\n<li>Specific rotation of the <strong>mixture<\/strong>: <strong>\u201340.58\u00b0<\/strong><\/li>\n<\/ul>\n\n\n\n<p>The formula for <strong>enantiomeric excess (ee)<\/strong> is: ee=(observed&nbsp;rotationrotation&nbsp;of&nbsp;pure&nbsp;enantiomer)\u00d7100%ee = \\left( \\frac{\\text{observed rotation}}{\\text{rotation of pure enantiomer}} \\right) \\times 100\\%<\/p>\n\n\n\n<p>Since the observed rotation is negative, we take the value for (R)-Carvone as the pure enantiomer reference: ee=(\u221240.58\u221261)\u00d7100%=66.52%ee = \\left( \\frac{-40.58}{-61} \\right) \\times 100\\% = 66.52\\%<\/p>\n\n\n\n<p>\u2705 <strong>Correct answer for Part I: e) 66.52<\/strong><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h3 class=\"wp-block-heading\"><strong>Part II: What is the percentage of each enantiomer?<\/strong><\/h3>\n\n\n\n<p>Enantiomeric excess (ee) also means the <strong>excess percentage of one enantiomer over the racemic mixture<\/strong>. That is: ee=%major&nbsp;enantiomer\u2212%minor&nbsp;enantiomer\\text{ee} = \\% \\text{major enantiomer} &#8211; \\% \\text{minor enantiomer}<\/p>\n\n\n\n<p>And since the total must be 100%: %major+%minor=100%\\% \\text{major} + \\% \\text{minor} = 100\\%<\/p>\n\n\n\n<p>Let\u2019s solve this: %major\u2212%minor=66.52%major+%minor=100\\% \\text{major} &#8211; \\% \\text{minor} = 66.52 \\\\ \\% \\text{major} + \\% \\text{minor} = 100<\/p>\n\n\n\n<p>Add both equations: 2\u00d7%major=166.52\u21d2%major=83.26%%minor=100\u221283.26=16.74%2 \\times \\% \\text{major} = 166.52 \\Rightarrow \\% \\text{major} = 83.26\\% \\\\ \\% \\text{minor} = 100 &#8211; 83.26 = 16.74\\%<\/p>\n\n\n\n<p>Since the mixture has a <strong>negative rotation<\/strong>, the <strong>(R)-Carvone<\/strong> is in excess.<\/p>\n\n\n\n<p>\u2705 <strong>(R)-Carvone: 83.26%<\/strong>, <strong>(S)-Carvone: 16.74%<\/strong><\/p>\n\n\n\n<p>So the correct answer for <strong>Part II<\/strong> is:<\/p>\n\n\n\n<p><strong>e) 83.26% of (R) and 16.74% of (S)<\/strong><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<h3 class=\"wp-block-heading\">\u2705 Final Answers:<\/h3>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Part I:<\/strong> e) <strong>66.52<\/strong><\/li>\n\n\n\n<li><strong>Part II:<\/strong> e) <strong>83.26% of (R) and 16.74% of (S)<\/strong><\/li>\n<\/ul>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" src=\"https:\/\/learnexams.com\/blog\/wp-content\/uploads\/2025\/05\/learnexams-banner6-156.jpeg\" alt=\"\" class=\"wp-image-222026\"\/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>The specific rotation of -Carvone is +61 degrees, while the specific rotation of (R)-Carvone is -61 degrees. If a sample of mixture of the two enantiomers has a specific rotation of -40.58 degrees Part I. What is the percent enantiomeric excess of the mixture?a) +24.75b) -24.75c) 24.75d) -66.52e) 66.52 Part II. What is the percentage [&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 center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[25],"tags":[],"class_list":["post-222024","post","type-post","status-publish","format-standard","hentry","category-exams-certification"],"_links":{"self":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/posts\/222024","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/comments?post=222024"}],"version-history":[{"count":0,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/posts\/222024\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/media?parent=222024"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/categories?post=222024"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.learnexams.com\/blog\/wp-json\/wp\/v2\/tags?post=222024"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}