{"id":25501,"date":"2023-02-21T19:23:10","date_gmt":"2023-02-21T19:23:10","guid":{"rendered":"https:\/\/notes.aayo.blog\/?p=25501"},"modified":"2023-08-01T15:35:37","modified_gmt":"2023-08-01T15:35:37","slug":"nitro-compounds","status":"publish","type":"post","link":"https:\/\/notes.aayo.blog\/index.php\/2023\/02\/21\/nitro-compounds\/","title":{"rendered":"NITRO COMPOUNDS"},"content":{"rendered":"\n<h3 class=\"wp-block-heading\">Introduction <\/h3>\n\n\n\n<p>Organic compounds containing nitro (\u2500NO2) group as the functional group are called nitro compounds.<br>General Formula<\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img fetchpriority=\"high\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-27.png\" alt=\"\" class=\"wp-image-25938\" width=\"570\" height=\"174\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-27.png 708w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-27-300x92.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-27-600x183.png 600w\" sizes=\"(max-width: 570px) 100vw, 570px\" \/><\/figure>\n\n\n\n<p><strong>Structure of -NO2 functional group<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-28.png\" alt=\"\" class=\"wp-image-25939\" width=\"638\" height=\"218\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-28.png 782w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-28-300x102.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-28-768x262.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-28-600x205.png 600w\" sizes=\"(max-width: 638px) 100vw, 638px\" \/><\/figure>\n\n\n\n<p><strong>Isomeric form of -NO2 functional group<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-29.png\" alt=\"\" class=\"wp-image-25940\" width=\"524\" height=\"179\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-29.png 712w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-29-300x102.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-29-600x205.png 600w\" sizes=\"(max-width: 524px) 100vw, 524px\" \/><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\">Classification of nitro compounds<\/h3>\n\n\n\n<p>Nitro compounds are broadly classified into two types;<\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-30.png\" alt=\"\" class=\"wp-image-25941\" width=\"704\" height=\"248\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-30.png 997w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-30-300x106.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-30-768x270.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-30-600x211.png 600w\" sizes=\"(max-width: 704px) 100vw, 704px\" \/><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\">Examples with IUPAC Nomenclature<\/h3>\n\n\n\n<p><strong>a)Aliphatic Nitro compounds<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-31.png\" alt=\"\" class=\"wp-image-25942\" width=\"515\" height=\"218\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-31.png 858w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-31-300x127.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-31-768x325.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-31-600x254.png 600w\" sizes=\"(max-width: 515px) 100vw, 515px\" \/><figcaption class=\"wp-element-caption\"><strong>b) Aromatic Nitro Compounds<\/strong><\/figcaption><\/figure>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-32.png\" alt=\"\" class=\"wp-image-25943\" width=\"510\" height=\"356\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-32.png 1007w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-32-300x209.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-32-768x535.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-32-600x418.png 600w\" sizes=\"(max-width: 510px) 100vw, 510px\" \/><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\">Isomerism in aliphatic nitro compounds<\/h3>\n\n\n\n<p><strong>Isomers of C2H5NO2<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-33.png\" alt=\"\" class=\"wp-image-25944\" width=\"396\" height=\"96\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-33.png 557w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-33-300x73.png 300w\" sizes=\"(max-width: 396px) 100vw, 396px\" \/><\/figure>\n\n\n\n<p><br><strong>Isomers of C2H5NO2<\/strong><br>Isomer I &amp;II compared with isomers III &amp; IV are chain isomers of each other<\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-34.png\" alt=\"\" class=\"wp-image-25945\" width=\"602\" height=\"529\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-34.png 857w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-34-300x264.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-34-768x675.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-34-600x527.png 600w\" sizes=\"(max-width: 602px) 100vw, 602px\" \/><\/figure>\n\n\n\n<p><\/p>\n\n\n\n<h3 class=\"wp-block-heading\">General Method of preparation of aliphatic nitro compounds<\/h3>\n\n\n\n<p><strong>a)From haloalkane<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-35.png\" alt=\"\" class=\"wp-image-25946\" width=\"622\" height=\"193\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-35.png 941w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-35-300x93.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-35-768x238.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-35-600x186.png 600w\" sizes=\"(max-width: 622px) 100vw, 622px\" \/><\/figure>\n\n\n\n<p>Note: When alcoholic solution of KNO2 or NaNO2 is used then alkyl nitrite is the major product because negatively charged oxygen atom acts as nucleophile whereas when alcoholic solution of AgNO2 is used then nitroalkane is the major product because N- atom with lone pair electron acts as nucleophile<\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-36.png\" alt=\"\" class=\"wp-image-25947\" width=\"760\" height=\"118\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-36.png 927w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-36-300x47.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-36-768x119.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-36-600x93.png 600w\" sizes=\"(max-width: 760px) 100vw, 760px\" \/><\/figure>\n\n\n\n<p><strong>b) From alkane<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-37.png\" alt=\"\" class=\"wp-image-25948\" width=\"614\" height=\"104\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-37.png 962w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-37-300x51.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-37-768x130.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-37-600x102.png 600w\" sizes=\"(max-width: 614px) 100vw, 614px\" \/><\/figure>\n\n\n\n<p>Note: Alkanes are difficult to nitrate and nitration results in the mixture of nitroalkanes because C-C bond of the alkane undergoes fission at high temperature.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Physical Properties of Nitroalkanes<\/h3>\n\n\n\n<p>i) State, Color and Odor: Nitroalkanes are colorless liquids with a pleasant odor.<br>ii) Solubility: Nitrobenzene are are slightly soluble in water while completely soluble in organic solvents.<br>iii) Boiling points: Nitroalkanes are polar in nature. Due to strong dipole-dipole interactions, these compounds show higher boiling points than the hydrocarbons of comparable molecular mass.<br>But lower boiling points than the alcohols and carboxylic acids of comparable<br>molecular mass due to absence of intermolecular H-bonding in nitroalkanes.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Chemical Properties of Nitroalkanes<\/h3>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-38.png\" alt=\"\" class=\"wp-image-25949\" width=\"673\" height=\"524\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-38.png 995w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-38-300x234.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-38-768x598.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-38-600x467.png 600w\" sizes=\"(max-width: 673px) 100vw, 673px\" \/><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\">Aromatic Nitro compounds<\/h3>\n\n\n\n<p><strong>Nitrobenzene (Oil of mirbane<\/strong>)<\/p>\n\n\n\n<p>Molecular formula: C6H5-<br>NO2 Structure:<\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-39.png\" alt=\"\" class=\"wp-image-25950\" width=\"469\" height=\"208\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-39.png 661w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-39-300x133.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-39-600x266.png 600w\" sizes=\"(max-width: 469px) 100vw, 469px\" \/><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\">Preparation of Nitrobenzene from Benzene<\/h3>\n\n\n\n<p>Nitrobenzene is prepared in laboratory by heating benzene with nitrating mixture (Conc.HNO3+ Conc. H2SO4) up to 60\u00b0C. This reaction is called nitration of benzene. It is an electrophilic substitution reaction. In This reaction nitronium ion (NO+2) acts as an electrophile produced from the reaction of nitrating mixture. Conc H2SO4 acts as acid and conc. HNO3 acts like base.<\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-40.png\" alt=\"\" class=\"wp-image-25951\" width=\"575\" height=\"204\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-40.png 846w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-40-300x106.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-40-768x272.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-40-600x213.png 600w\" sizes=\"(max-width: 575px) 100vw, 575px\" \/><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\">Physical properties of Nitrobenzene<\/h3>\n\n\n\n<p>i) Nitrobenzene is a pale-yellow oily liquid with bitter almond smell. It is also called \u201coil of Mirbane\u201d<br>ii) It boils at 210\u00b0C.<br>iii) It is insoluble in water and soluble in organic solvents.<br>iv) It is a toxic compound since its vapors are absorbed through skin.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Chemical properties of Nitrobenzene<\/h3>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-43.png\" alt=\"\" class=\"wp-image-25954\" width=\"573\" height=\"489\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-43.png 758w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-43-300x256.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-43-600x512.png 600w\" sizes=\"(max-width: 573px) 100vw, 573px\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-44.png\" alt=\"\" class=\"wp-image-25955\" width=\"602\" height=\"352\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-44.png 917w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-44-300x175.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-44-768x449.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-44-600x351.png 600w\" sizes=\"(max-width: 602px) 100vw, 602px\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-45.png\" alt=\"\" class=\"wp-image-25956\" width=\"720\" height=\"524\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-45.png 985w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-45-300x218.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-45-768x559.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-45-600x437.png 600w\" sizes=\"(max-width: 720px) 100vw, 720px\" \/><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\">Electrophilic Substitution Reaction (ESR) in Nitrobenzene:<\/h3>\n\n\n\n<p>Nitrobenzene undergoes electrophilic substitution reaction at meta-position. This is because-NO2 group present in nitrobenzene is electron withdrawing and m-director in nature. Due to resonance in nitrobenzene, the electron density at ortho and para position decreases as compared to meta-position. Therefore, the incoming electrophile will prefer to attack meta-position in nitrobenzene<\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-46.png\" alt=\"\" class=\"wp-image-25957\" width=\"713\" height=\"256\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-46.png 981w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-46-300x108.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-46-768x276.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-46-600x215.png 600w\" sizes=\"(max-width: 713px) 100vw, 713px\" \/><\/figure>\n\n\n\n<p>Some electrophilic substitution reactions of nitrobenzene are as follows<\/p>\n\n\n\n<figure class=\"wp-block-image size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-47.png\" alt=\"\" class=\"wp-image-25958\" width=\"728\" height=\"640\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-47.png 992w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-47-300x264.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-47-768x675.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-47-600x527.png 600w\" sizes=\"(max-width: 728px) 100vw, 728px\" \/><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\">Uses of Nitro compounds<\/h3>\n\n\n\n<p>i) It is used for the preparation of dyes and explosives such as TNB (1,3,5-trinitrobenzene),<br>TNT (1,3,5-trinitrotoluene), etc.<br>ii) It is a precursor molecule in the manufacture of Aniline.<br>iii) It is used as solvent in making shoe polish.<br>iv) It is used as scenting material for making cheap soaps,<br>v) It is used to synthesize \u201cartificial musk like odor\u201d perfume also called toluene musk.<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"773\" height=\"222\" src=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-49.png\" alt=\"\" class=\"wp-image-25960\" srcset=\"https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-49.png 773w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-49-300x86.png 300w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-49-768x221.png 768w, https:\/\/notes.aayo.blog\/wp-content\/uploads\/2023\/03\/image-49-600x172.png 600w\" sizes=\"(max-width: 773px) 100vw, 773px\" \/><\/figure>\n\n\n\n<p><\/p>\n\n\n\n<p><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Introduction Organic compounds containing nitro (\u2500NO2) group as the functional group are called nitro compounds.General Formula Structure of -NO2 functional group Isomeric form of -NO2 functional group Classification of nitro compounds Nitro compounds are broadly classified into two types; Examples with IUPAC Nomenclature a)Aliphatic Nitro compounds Isomerism in aliphatic nitro compounds Isomers of C2H5NO2 Isomers [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":26020,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_uag_custom_page_level_css":"","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":"disabled","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":"var(--ast-global-color-4)","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":[1],"tags":[43],"class_list":["post-25501","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized","tag-nitrocompound"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Nitro Compounds Notes -Grade 12 [NEB]<\/title>\n<meta name=\"description\" content=\"Here, we have posted notes of Nitro Compounds Grade 12 NEB . 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