{"id":776,"date":"2010-08-27T16:00:10","date_gmt":"2010-08-27T14:00:10","guid":{"rendered":"http:\/\/masterorganicchemistry.wordpress.com\/?p=776"},"modified":"2025-01-23T13:59:29","modified_gmt":"2025-01-23T19:59:29","slug":"common-mistakes-pentavalent-carbon","status":"publish","type":"post","link":"https:\/\/www.masterorganicchemistry.com\/2010\/08\/27\/common-mistakes-pentavalent-carbon\/","title":{"rendered":"Common Mistakes in Organic Chemistry: Pentavalent Carbon"},"content":{"rendered":"<p><strong>Pentavalent (a.k.a. &#8220;Texas&#8221;) Carbons<\/strong><\/p>\n<p>So what are some of the most common mistakes we can make in organic chemistry?<\/p>\n<p>Given the relatively <em>qualitative <\/em>nature of sophomore organic chemistry, it should not be surprising that there is truly an astonishing variety of ways to screw things up. Today I&#8217;l just mention one mistake in particular, but it is probably the biggest mistake of them all &#8211; <strong>drawing 5 bonds on carbon.<\/strong><\/p>\n<p><img fetchpriority=\"high\" decoding=\"async\" class=\"alignnone wp-image-38659\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2025\/01\/0-Mistakes-pentavalent-carbons-texas-carbons-common-mistakes.gif\" alt=\"Mistakes-pentavalent carbons texas carbons common mistakes\" width=\"640\" height=\"514\" \/><\/a><\/p>\n<p>Among those of us in the field, 5-bonded carbon &#8211; pentavalent carbon &#8211; goes by another popular nickname: <strong>Texas carbon<\/strong>. Why? A picture makes it pretty self-explanatory.<\/p>\n<p><img decoding=\"async\" class=\"aligncenter wp-image-14233\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2019\/12\/1-texas-flag-with-pentavalent-carbon-included.jpg\" alt=\"texas-flag-with-pentavalent-carbon-included\" width=\"375\" height=\"250\" srcset=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2019\/12\/1-texas-flag-with-pentavalent-carbon-included.jpg 414w, https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2019\/12\/1-texas-flag-with-pentavalent-carbon-included-300x200.jpg 300w, https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2019\/12\/1-texas-flag-with-pentavalent-carbon-included-320x213.jpg 320w, https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2019\/12\/1-texas-flag-with-pentavalent-carbon-included-360x240.jpg 360w\" sizes=\"(max-width: 375px) 100vw, 375px\" \/><\/p>\n<p>While Texas carbon that resembles the emblem of the Lone Star State is the easiest to spot, there are other, more subtle variations. Let&#8217;s look at a few.<\/p>\n<p><img decoding=\"async\" class=\"aligncenter wp-image-14234\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2019\/12\/2-examples-of-pentavalent-carbon-drawing-mistakes.gif\" alt=\"examples-of-pentavalent-carbon-drawing-mistakes\" width=\"601\" height=\"275\" \/><\/p>\n<p>What are the key principles at work here?<\/p>\n<h2><strong>1. The number of bonds to carbon cannot exceed four<\/strong><\/h2>\n<p>Carbon has a single 2s orbital and three 2 p orbitals available in its valence shell, and thus can form a maximum of four bonds. While this might be easy to spot in the case of the &#8220;lone star&#8221; variant, it&#8217;s a little trickier to see in the context of sp<sup>2<\/sup> and sp<sup>3<\/sup> carbons, especially for the beginner.<\/p>\n<p><span style=\"color: #993366;\"><em>Probably the most difficult pentavalent carbon to spot is in condensed structural formulas, where the bonds aren&#8217;t explicitly drawn out.<\/em> <\/span><\/p>\n<p>Mistakes such as CH<sub>3<\/sub>CH<sub>2<\/sub>(CH<sub>3<\/sub>)<sub>2<\/sub> can be easy to make and hard to find.<\/p>\n<h2><strong>2. The number of <\/strong><strong>orbitals<\/strong><strong> around carbon cannot exceed four<\/strong><\/h2>\n<p>Part of the confusion here stems from the inherent laziness\u00a0 of chemists in depicting chemical structures: we often neglect to draw in lone pairs and C\u2013H bonds, but you&#8217;re just supposed to remember that they&#8217;re there. (<span style=\"color: #993366;\"><em>See article: <a href=\"https:\/\/www.masterorganicchemistry.com\/2011\/06\/27\/hidden-hydrogens-hidden-lone-pairs-hidden-counterions\/\">Hidden Hydrogens, Hidden Lone Pairs, Hidden Hydrogens<\/a><\/em><\/span>)<\/p>\n<p>Remember that a negative charge (\u2013) signifies a lone pair of electrons around carbon, <strong>even if the lone pair isn&#8217;t explicitly drawn in<\/strong>. This occupies an orbital.<\/p>\n<p>Likewise, when you see a (+) drawn beside a carbon, that implies the existence of an empty orbital around the carbon. Hence the &#8220;anionic&#8221; and &#8220;cationic&#8221; variants drawn are also examples of forbidden carbons.<\/p>\n<h2><strong>3. The same principles apply for other first-row elements<\/strong><\/h2>\n<p>Oxygen and nitrogen (and fluorine and boron, for that matter) cannot exceed the maximum of four orbitals\/eight electrons either.<br \/>\n<img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-14235\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2019\/12\/3-examples-of-drawing-mistakes-oxygen-and-nitrogen-breaking-octet-rule.gif\" alt=\"examples-of-drawing-mistakes-oxygen-and-nitrogen-breaking-octet-rule\" width=\"585\" height=\"138\" \/><\/p>\n<p>A word of advice, especially for exams: <strong>paranoia<\/strong>. \u00a0This can be an exceptionally easy mistake to make, but you&#8217;ll get better at spotting these things with practice.<\/p>\n<p>Trust me: your professor, your TA, and everyone else who has ever taken organic chemistry has made this mistake at some point. I&#8217;ve done this myself too many times to count.<\/p>\n<p>One never gains a magic ability to avoid drawing Texas carbons, but over time, like with most things, a certain low-level fear sets in that helps to catch these mistakes right after they happen.\u00a0 If one of the world&#8217;s most outstanding chemists can <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.200502178\/full\">miss<\/a> seeing a pentavalent carbon, anyone can.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-14236\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2019\/12\/4-anionic-and-cationic-carbon-octet-rule-violations.gif\" alt=\"anionic-and-cationic-carbon-octet-rule-violations\" width=\"585\" height=\"138\" \/><\/p>\n<h2>4. Spot The Mistakes<\/h2>\n<p>When Hollywood or a video game or even some graphic designer decides they need to draw a picture of a molecule, it seems like they just look at a few pictures of benzene online for inspiration and then start adding random extra bonds to improve the molecule&#8217;s &#8220;vibe&#8221;. This inevitably results in physically impossible molecular structures which, in addition to providing a source of amusement for organic chemists, are excellent quiz material.<\/p>\n<p>Case in point. This molecule is found somewhere in <em>Call of Duty: Black Ops 3 (hat tip: r\/chemistry). <\/em>I&#8217;m not certain of the exact context, but the game \u00a0&#8220;deploys its players into a future where bio-technology has enabled a new breed of Black Ops soldier.&#8221;<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-38676\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2025\/01\/5-molecule-from-call-of-duty-black-ops-3-with-impossible-structure.jpg\" alt=\"molecule from call of duty black ops 3 with impossible structure\" width=\"450\" height=\"675\" srcset=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2025\/01\/5-molecule-from-call-of-duty-black-ops-3-with-impossible-structure.jpg 1080w, https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2025\/01\/5-molecule-from-call-of-duty-black-ops-3-with-impossible-structure-200x300.jpg 200w, https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2025\/01\/5-molecule-from-call-of-duty-black-ops-3-with-impossible-structure-683x1024.jpg 683w, https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2025\/01\/5-molecule-from-call-of-duty-black-ops-3-with-impossible-structure-768x1152.jpg 768w, https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2025\/01\/5-molecule-from-call-of-duty-black-ops-3-with-impossible-structure-1024x1536.jpg 1024w, https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2025\/01\/5-molecule-from-call-of-duty-black-ops-3-with-impossible-structure-507x760.jpg 507w\" sizes=\"(max-width: 450px) 100vw, 450px\" \/><\/a><\/p>\n<p>No kidding. I mean, where do you even start with this? Can you spot the\u00a0<strong>heptavalent<\/strong><em>\u00a0<\/em>carbon?<\/p>\n<p>Here&#8217;s some more quizzes on spotting pentavalent carbons.<\/p>\n<p><div class=\"wq-quiz-wrapper\" data-id=\"38672\"><style type=\"text\/css\" id=\"wq-flip-custom-css\">.wq-quiz-wrapper[data-id=\"38672\"] {\n--wq-question-width: 100%;\n--wq-question-color: #009cff;\n--wq-question-height: auto;\n--wq-font-color: #444;\n}\n\n\t\t\t.wq-quiz-wrapper[data-id=\"38672\"] {\n\t\t\t\t--wq-question-width: 600px;\n\t\t\t}\n\n\t\t\t@media screen and (max-width: 600px) {\n\t\t\t\t.wq-quiz-wrapper[data-id=\"38672\"] .wq_singleQuestionWrapper { width:100% !important; height:auto !important; }\n\t\t\t}\n\t\t<\/style><!-- wp quiz -->\n<div id=\"wp-quiz-38672\" class=\"wq_quizCtr single flip_quiz wq-quiz wq-quiz-38672 wq-quiz-flip wq-layout-single wq-skin-traditional wq-should-show-correct-answer\" data-quiz-id=\"38672\">\n<div class=\"wq-questions wq_questionsCtr\">\n\t<div class=\"wq-question wq_singleQuestionWrapper wq-question-lmy22\" data-id=\"lmy22\">\n\n\t\n\t<div class=\"item_top\">\n\t\t<div class=\"title_container\">\n\t\t\t<div class=\"wq_questionTextCtr\">\n\t\t\t\t<h4 class=\"wq-question-title\"><\/h4>\n\t\t\t<\/div>\n\t\t<\/div>\n\t<\/div>\n\n\t<div class=\"card \">\n\t\t<div class=\"front\" >\n\t\n\t\t\t\t\t<img decoding=\"async\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/quiz-images\/3023-Front.gif\" \/>\n\t\t\n\t\t\n\t\n\t\n\t\t\t<span class=\"top-desc\">Click to Flip<\/span>\n\t<\/div>\n\t\t<div class=\"back\" >\n\t\n\t\t\t\t\t<img decoding=\"async\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/quiz-images\/3023-Reverse.gif\" \/>\n\t\t\n\t\t\n\t\n\t<\/div>\n\t<\/div>\n\n\t\n<\/div>\n<\/div>\n<\/div>\n<!-- \/\/ wp quiz-->\n<\/div><!-- End .wq-quiz-wrapper --><br \/>\n<div class=\"wq-quiz-wrapper\" data-id=\"38673\"><style type=\"text\/css\" id=\"wq-flip-custom-css\">.wq-quiz-wrapper[data-id=\"38673\"] {\n--wq-question-width: 100%;\n--wq-question-color: #009cff;\n--wq-question-height: auto;\n--wq-font-color: #444;\n}\n\n\t\t\t.wq-quiz-wrapper[data-id=\"38673\"] {\n\t\t\t\t--wq-question-width: 600px;\n\t\t\t}\n\n\t\t\t@media screen and (max-width: 600px) {\n\t\t\t\t.wq-quiz-wrapper[data-id=\"38673\"] .wq_singleQuestionWrapper { width:100% !important; height:auto !important; }\n\t\t\t}\n\t\t<\/style><!-- wp quiz -->\n<div id=\"wp-quiz-38673\" class=\"wq_quizCtr single flip_quiz wq-quiz wq-quiz-38673 wq-quiz-flip wq-layout-single wq-skin-traditional wq-should-show-correct-answer\" data-quiz-id=\"38673\">\n<div class=\"wq-questions wq_questionsCtr\">\n\t<div class=\"wq-question wq_singleQuestionWrapper wq-question-pjvcx\" data-id=\"pjvcx\">\n\n\t\n\t<div class=\"item_top\">\n\t\t<div class=\"title_container\">\n\t\t\t<div class=\"wq_questionTextCtr\">\n\t\t\t\t<h4 class=\"wq-question-title\"><\/h4>\n\t\t\t<\/div>\n\t\t<\/div>\n\t<\/div>\n\n\t<div class=\"card \">\n\t\t<div class=\"front\" >\n\t\n\t\t\t\t\t<img decoding=\"async\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/quiz-images\/3024-Front.gif\" \/>\n\t\t\n\t\t\n\t\n\t\n\t\t\t<span class=\"top-desc\">Click to Flip<\/span>\n\t<\/div>\n\t\t<div class=\"back\" >\n\t\n\t\t\t\t\t<img decoding=\"async\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/quiz-images\/3024-Reverse.gif\" \/>\n\t\t\n\t\t\n\t\n\t<\/div>\n\t<\/div>\n\n\t\n<\/div>\n<\/div>\n<\/div>\n<!-- \/\/ wp quiz-->\n<\/div><!-- End .wq-quiz-wrapper --><br \/>\n<div class=\"wq-quiz-wrapper\" data-id=\"38674\"><style type=\"text\/css\" id=\"wq-flip-custom-css\">.wq-quiz-wrapper[data-id=\"38674\"] {\n--wq-question-width: 100%;\n--wq-question-color: #009cff;\n--wq-question-height: auto;\n--wq-font-color: #444;\n}\n\n\t\t\t.wq-quiz-wrapper[data-id=\"38674\"] {\n\t\t\t\t--wq-question-width: 600px;\n\t\t\t}\n\n\t\t\t@media screen and (max-width: 600px) {\n\t\t\t\t.wq-quiz-wrapper[data-id=\"38674\"] .wq_singleQuestionWrapper { width:100% !important; height:auto !important; }\n\t\t\t}\n\t\t<\/style><!-- wp quiz -->\n<div id=\"wp-quiz-38674\" class=\"wq_quizCtr single flip_quiz wq-quiz wq-quiz-38674 wq-quiz-flip wq-layout-single wq-skin-traditional wq-should-show-correct-answer\" data-quiz-id=\"38674\">\n<div class=\"wq-questions wq_questionsCtr\">\n\t<div class=\"wq-question wq_singleQuestionWrapper wq-question-kk474\" data-id=\"kk474\">\n\n\t\n\t<div class=\"item_top\">\n\t\t<div class=\"title_container\">\n\t\t\t<div class=\"wq_questionTextCtr\">\n\t\t\t\t<h4 class=\"wq-question-title\"><\/h4>\n\t\t\t<\/div>\n\t\t<\/div>\n\t<\/div>\n\n\t<div class=\"card \">\n\t\t<div class=\"front\" >\n\t\n\t\t\t\t\t<img decoding=\"async\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/quiz-images\/3025-Front.gif\" \/>\n\t\t\n\t\t\n\t\n\t\n\t\t\t<span class=\"top-desc\">Click to Flip<\/span>\n\t<\/div>\n\t\t<div class=\"back\" >\n\t\n\t\t\t\t\t<img decoding=\"async\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/quiz-images\/3025-Reverse.gif\" \/>\n\t\t\n\t\t\n\t\n\t<\/div>\n\t<\/div>\n\n\t\n<\/div>\n<\/div>\n<\/div>\n<!-- \/\/ wp quiz-->\n<\/div><!-- End .wq-quiz-wrapper --><\/p>\n<hr \/>\n<h2><a id=\"notes\"><\/a>Notes<\/h2>\n<div class=\"related-articles\"><p><strong>Related Articles<\/strong><\/p><ul><li><a href=\"https:\/\/www.masterorganicchemistry.com\/2011\/02\/14\/table-of-functional-group-priorities-for-nomenclature\/\" class=\"\"><span>Table of Functional Group Priorities for Nomenclature<\/span><\/a><\/li><li><a href=\"https:\/\/www.masterorganicchemistry.com\/2012\/02\/22\/common-mistakes-formal-charges-can-mislead\/\" class=\"\"><span>Common Mistakes: Formal Charges Can Mislead<\/span><\/a><\/li><li><a href=\"https:\/\/www.masterorganicchemistry.com\/2013\/03\/12\/common-mistakes-drawing-tetrahedral-carbons\/\" class=\"\"><span>Wedge And Dash Convention For Tetrahedral Carbon<\/span><\/a><\/li><li><a href=\"https:\/\/www.masterorganicchemistry.com\/2011\/06\/27\/hidden-hydrogens-hidden-lone-pairs-hidden-counterions\/\" class=\"\"><span>Hidden Hydrogens, Hidden Lone Pairs, Hidden Counterions<\/span><\/a><\/li><li><a href=\"https:\/\/www.masterorganicchemistry.com\/2010\/09\/24\/how-to-calculate-formal-charge\/\" class=\"\"><span>A Key Skill: How to Calculate Formal Charge<\/span><\/a><\/li><li><a href=\"https:\/\/www.masterorganicchemistry.com\/2017\/08\/25\/how-do-we-know-methane-is-tetrahedral\/\" class=\"\"><span>How Do We Know Methane (CH4) Is Tetrahedral?<\/span><\/a><\/li><li><a href=\"https:\/\/www.masterorganicchemistry.com\/2018\/01\/16\/a-hybridization-shortcut\/\" class=\"\"><span>How To Determine Hybridization: A Shortcut<\/span><\/a><\/li><\/ul><\/div>\n<p style=\"text-align: left;\"><strong>Note 1.\u00a0<\/strong><a href=\"https:\/\/m.xkcd.com\/3040\/\">XKCD comic<\/a> on &#8220;How To Annoy Chemists&#8221; has a whopper. Can you spot it?<\/p>\n<p><strong><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-38706 size-full\" src=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2010\/08\/F1-XKCD-3040-texas-carbon-incorrect-drawing-of-penta-coordinate-carbon-in-xkcd-breaks-the-octet-rule.jpg\" alt=\"XKCD 3040 texas carbon incorrect drawing of penta coordinate carbon in xkcd breaks the octet rule\" width=\"551\" height=\"669\" srcset=\"https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2010\/08\/F1-XKCD-3040-texas-carbon-incorrect-drawing-of-penta-coordinate-carbon-in-xkcd-breaks-the-octet-rule.jpg 551w, https:\/\/www.masterorganicchemistry.com\/wp-content\/uploads\/2010\/08\/F1-XKCD-3040-texas-carbon-incorrect-drawing-of-penta-coordinate-carbon-in-xkcd-breaks-the-octet-rule-247x300.jpg 247w\" sizes=\"(max-width: 551px) 100vw, 551px\" \/><\/a><\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Pentavalent (a.k.a. &#8220;Texas&#8221;) Carbons So what are some of the most common mistakes we can make in organic chemistry? Given the relatively qualitative nature of <\/p>\n","protected":false},"author":1,"featured_media":38659,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[1408],"tags":[566,196,419,236,242,699,711,710],"post_folder":[],"class_list":["post-776","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-alkanes-nomenclature","tag-blind-spots","tag-conventions","tag-fun","tag-mistakes","tag-nomenclature","tag-octet-rule","tag-pentavalent","tag-texas"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Common Mistakes in Organic Chemistry: Pentavalent Carbon &#8211; Master Organic Chemistry<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.masterorganicchemistry.com\/2010\/08\/27\/common-mistakes-pentavalent-carbon\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Common Mistakes in Organic Chemistry: Pentavalent Carbon &#8211; Master Organic Chemistry\" \/>\n<meta property=\"og:description\" content=\"Pentavalent (a.k.a. &#8220;Texas&#8221;) Carbons So what are some of the most common mistakes we can make in organic chemistry? 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