{"id":148982,"date":"2024-02-27T19:16:23","date_gmt":"2024-02-27T13:46:23","guid":{"rendered":"https:\/\/www.mapsofindia.com\/my-india\/?p=148982"},"modified":"2024-02-27T19:16:23","modified_gmt":"2024-02-27T13:46:23","slug":"arrange-the-following-compounds-in-the-increasing-order-of-their-basic","status":"publish","type":"post","link":"https:\/\/www.mapsofindia.com\/my-india\/quiz\/arrange-the-following-compounds-in-the-increasing-order-of-their-basic","title":{"rendered":"Arrange the following compounds in the increasing order of their basic&#8230;"},"content":{"rendered":"<h3>Arrange the following compounds in the increasing order of their basic strength in gaseous phase :<br \/>\nC2H5NH2,(C2H5)3N,(C2H5)2NH<\/h3>\n<h3>Ans.<\/h3>\n<h3>To determine the increasing order of basic strength of the given compounds in the gaseous phase, we need to consider the structures and steric hindrance effects of the compounds.<\/h3>\n<h3>The basic strength of an amine depends on the availability of the lone pair of electrons on the nitrogen atom. Generally, the greater the availability of the lone pair, the stronger the base.<\/h3>\n<h3>Here are the structures of the given compounds:<\/h3>\n<ol>\n<li>\n<h3><span class=\"math math-inline\"><span class=\"katex\"><span class=\"katex-mathml\">\ufffd2\ufffd5\ufffd\ufffd2<\/span><span class=\"katex-html\" aria-hidden=\"true\"><span class=\"base\"><span class=\"mord\"><span class=\"mord mathnormal\">C<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">5<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">N<\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/span> (Ethylamine)<\/h3>\n<\/li>\n<li>\n<h3><span class=\"math math-inline\"><span class=\"katex\"><span class=\"katex-mathml\">(\ufffd2\ufffd5)3\ufffd<\/span><span class=\"katex-html\" aria-hidden=\"true\"><span class=\"base\"><span class=\"mopen\">(<\/span><span class=\"mord\"><span class=\"mord mathnormal\">C<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">5<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mclose\">)<span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">3<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">N<\/span><\/span><\/span><\/span><\/span> (Triethylamine)<\/h3>\n<\/li>\n<li>\n<h3><span class=\"math math-inline\"><span class=\"katex\"><span class=\"katex-mathml\">(\ufffd2\ufffd5)2\ufffd\ufffd<\/span><span class=\"katex-html\" aria-hidden=\"true\"><span class=\"base\"><span class=\"mopen\">(<\/span><span class=\"mord\"><span class=\"mord mathnormal\">C<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">5<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mclose\">)<span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">N<\/span><span class=\"mord mathnormal\">H<\/span><\/span><\/span><\/span><\/span> (Diethylamine)<\/h3>\n<\/li>\n<\/ol>\n<h3>Now, let&#8217;s analyze:<\/h3>\n<ul>\n<li>\n<h3>Ethylamine (<span class=\"math math-inline\"><span class=\"katex\"><span class=\"katex-mathml\">\ufffd2\ufffd5\ufffd\ufffd2<\/span><span class=\"katex-html\" aria-hidden=\"true\"><span class=\"base\"><span class=\"mord\"><span class=\"mord mathnormal\">C<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">5<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">N<\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/span>): It is a primary amine with one ethyl group attached to the nitrogen atom. There is no steric hindrance around the nitrogen atom, so the lone pair is readily available for donation. Thus, it is the strongest base among the given compounds.<\/h3>\n<\/li>\n<li>\n<h3>Diethylamine (<span class=\"math math-inline\"><span class=\"katex\"><span class=\"katex-mathml\">(\ufffd2\ufffd5)2\ufffd\ufffd<\/span><span class=\"katex-html\" aria-hidden=\"true\"><span class=\"base\"><span class=\"mopen\">(<\/span><span class=\"mord\"><span class=\"mord mathnormal\">C<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">5<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mclose\">)<span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">N<\/span><span class=\"mord mathnormal\">H<\/span><\/span><\/span><\/span><\/span>): It is a secondary amine with two ethyl groups attached to the nitrogen atom. The presence of two ethyl groups causes some steric hindrance around the nitrogen atom, reducing the availability of the lone pair compared to ethylamine. Therefore, it is weaker than ethylamine.<\/h3>\n<\/li>\n<li>\n<h3>Triethylamine (<span class=\"math math-inline\"><span class=\"katex\"><span class=\"katex-mathml\">(\ufffd2\ufffd5)3\ufffd<\/span><span class=\"katex-html\" aria-hidden=\"true\"><span class=\"base\"><span class=\"mopen\">(<\/span><span class=\"mord\"><span class=\"mord mathnormal\">C<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">5<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mclose\">)<span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">3<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">N<\/span><\/span><\/span><\/span><\/span>): It is a tertiary amine with three ethyl groups attached to the nitrogen atom. Tertiary amines have the most steric hindrance around the nitrogen atom among the given compounds, which further reduces the availability of the lone pair. Thus, it is the weakest base among the given compounds.<\/h3>\n<\/li>\n<\/ul>\n<h3>Therefore, the increasing order of basic strength in the gaseous phase is: <span class=\"math math-inline\"><span class=\"katex\"><span class=\"katex-mathml\">\ufffd2\ufffd5\ufffd\ufffd2&gt;(\ufffd2\ufffd5)2\ufffd\ufffd&gt;(\ufffd2\ufffd5)3\ufffd<\/span><span class=\"katex-html\" aria-hidden=\"true\"><span class=\"base\"><span class=\"mord\"><span class=\"mord mathnormal\">C<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">5<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">N<\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mrel\">&gt;<\/span><\/span><span class=\"base\"><span class=\"mopen\">(<\/span><span class=\"mord\"><span class=\"mord mathnormal\">C<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">5<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mclose\">)<span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">N<\/span><span class=\"mord mathnormal\">H<\/span><span class=\"mrel\">&gt;<\/span><\/span><span class=\"base\"><span class=\"mopen\">(<\/span><span class=\"mord\"><span class=\"mord mathnormal\">C<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">2<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord\"><span class=\"mord mathnormal\">H<\/span><span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">5<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mclose\">)<span class=\"msupsub\"><span class=\"vlist-t vlist-t2\"><span class=\"vlist-r\"><span class=\"vlist\"><span class=\"sizing reset-size6 size3 mtight\"><span class=\"mord mtight\">3<\/span><\/span><\/span><span class=\"vlist-s\">\u200b<\/span><\/span><\/span><\/span><\/span><span class=\"mord mathnormal\">N<\/span><\/span><\/span><\/span><\/span><\/h3>\n","protected":false},"excerpt":{"rendered":"<p>Arrange the following compounds in the increasing order of their basic strength in gaseous phase : C2H5NH2,(C2H5)3N,(C2H5)2NH Ans. To determine the increasing order of basic strength of the given compounds in the gaseous phase, we need to consider the structures and steric hindrance effects of the compounds. The basic strength of an amine depends on [&hellip;]<\/p>\n","protected":false},"author":21830,"featured_media":114041,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[12119],"tags":[],"class_list":{"0":"post-148982","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-quiz"},"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/posts\/148982","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/users\/21830"}],"replies":[{"embeddable":true,"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/comments?post=148982"}],"version-history":[{"count":1,"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/posts\/148982\/revisions"}],"predecessor-version":[{"id":148983,"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/posts\/148982\/revisions\/148983"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/media\/114041"}],"wp:attachment":[{"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/media?parent=148982"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/categories?post=148982"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.mapsofindia.com\/my-india\/wp-json\/wp\/v2\/tags?post=148982"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}