{"id":638,"date":"2020-03-04T23:18:21","date_gmt":"2020-03-04T17:48:21","guid":{"rendered":"http:\/\/www.sbgstudy.com\/blog\/?p=638"},"modified":"2020-03-04T23:18:21","modified_gmt":"2020-03-04T17:48:21","slug":"chemistry-naming-reactions","status":"publish","type":"post","link":"https:\/\/sbgstudy.in\/blog\/chemistry-naming-reactions\/","title":{"rendered":"Chemistry Class 12 All Chemistry Naming Reactions  of Board Exam"},"content":{"rendered":"\n<p>Chemistry Class 12 All Chemistry Naming Reactions of Board Exam<\/p>\n\n\n\n<p>Here are some important chemical reactions which every student of class 12 must have a thorough understanding of.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">  Sandmeyer Reaction:  <\/h2>\n\n\n\n<ol class=\"wp-block-list\"><li>The Sandmeyer reaction is a chemical reaction that is used to synthesize aryl halides from aryl diazonium salts. This reaction is a method for substitution of an aromatic amino group by preparing diazonium salt that is followed by its displacement and copper salts often catalyze it. The Br, Cl and Cn nucleophiles can be easily present in the benzene ring of benzene diazonium salt in the presence of copper ion.<\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/1.png\" alt=\"Sandmeyer Reaction\" class=\"wp-image-4301\"\/><\/figure><\/div>\n\n\n\n<h2 class=\"wp-block-heading\"> Gattermann Reaction: <\/h2>\n\n\n\n<ol class=\"wp-block-list\"><li> Gattermann Reaction: Bromine and Chlorine can be present in the benzene ring by preparing the benzene diazonium salt solution with similar halogen acid present with copper powder. This is the Gattermann Reaction. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/2.png\" alt=\"Gattermann Reaction\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Balz-Schiemann Reaction: When arene-diazonium chloride is prepared with fluoroboric acid,  arene diazonium fluoroborate is precipitated and decomposes to yield  aryl fluoride which on heating. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/3.png\" alt=\"Balz-Schiemann Reaction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Finkelstein Reaction: In the Finkelstein Reaction Alkyl iodides are prepared easily by the reaction of alkyl chlorides with Nal in dry acetone. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/4.png\" alt=\"Finkelstein Reaction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Swarts Reaction: When alkyl chloride is heated in the presence of a metallic fluoride like AgF, Hg<sub>2<\/sub>F<sub>2<\/sub>, SbF<sub>3<\/sub> or CoF<sub>2<\/sub>, we get alkyl fluorides. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/5.png\" alt=\"Swarts Reaction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Wurtz Reaction: When Alkyl halides get reacted with sodium with dry ether, we get  hydrocarbons that include the double number of carbon atoms present in  the halide. This is known as the Wurtz Reaction<\/li><li> <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/6.png\" alt=\"Wurtz Reaction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Wurtz-Fittig Reaction: When a mixture of alkyl halide and aryl halide gets treated with sodium in dry ether, we get an alkyl arene. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/7.png\" alt=\"Wurtz-Fittig Reaction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Fittig Reaction: Aryl halides prepared with sodium in dry ether to give analogous compounds where two aryl groups joined. <\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/8.png\" alt=\"Fittig Reaction\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Friedel-Crafts alkylation Reaction: Benzene is prepared with an alkyl halide in the presence of anhydrous aluminum chloride to give Alkylbenzene. This is the Friedel-Crafts alkylation Reaction<\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/9.png\" alt=\"Friedel-Crafts alkylation Reaction\"\/><\/figure><\/div>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/9_1.png\" alt=\"Friedel-Crafts alkylation Reaction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/9_2.png\" alt=\"Friedel-Crafts alkylation Reaction\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Friedel-Crafts acylation reaction: We get acyl benzene when an acyl halide is reacted with benzene in the presence of Lewis acids.<br><br> <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/10_1.png\" alt=\"Friedel-Crafts acylation reaction\"\/><\/figure><\/div>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/10_2.png\" alt=\"Friedel-Crafts acylation reaction\"\/><\/figure><\/div>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/10_3.png\" alt=\"Friedel-Crafts acylation reaction\"\/><\/figure><\/div>\n\n\n\n<p>Also Read:\u00a0Acetylation<\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Reimer-Tiemann Reaction: When preparing phenol with chloroform in the presence of sodium  hydroxide, -CHO group is present at the ortho position of the benzene  ring which results into salicylaldehyde. <\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/11.png\" alt=\"Reimer-Tiemann Reaction\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Kolbe\u2019s Reaction: Phenol reacts with sodium hydroxide to give sodium phenoxide which  then reacts with carbon dioxide in acidic medium to give hydroxybenzoic  acid. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/12.png\" alt=\"Kolbe\u2019s Reaction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Rosenmund Reduction: When Acyl chloride is hydrogenated to an aldehyde over a catalyst, known as <strong>Rosenmund catalyst<\/strong> which is either palladium or <a href=\"https:\/\/byjus.com\/chemistry\/barium\/\">barium<\/a> sulfate. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/13.png\" alt=\"Rosenmund Reduction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Stephen reaction: Nitriles with stannous chloride in the presence of hydrochloric acid  reduced to the corresponding imine and give the corresponding aldehyde  after hydrolysis. <\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/14.png\" alt=\"Stephen reaction\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Etard reaction: Chromyl chloride oxidizes methyl group to get chromium complex which on hydrolysis provides corresponding benzaldehyde. <\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/15.png\" alt=\"Etard reaction\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Gatterman \u2013 Koch reaction: Benzene is prepared with carbon monoxide and hydrogen chloride in the  presence of anhydrous aluminum chloride to give benzaldehyde. <\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/16.png\" alt=\"Gatterman \u2013 Koch reaction\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Clemmensen Reduction: In Clemmensen reduction, Carbonyl group of aldehydes and ketones on treatment with zinc-amalgam and concentrated hydrochloric acid reduced to CH<sub>2<\/sub> group. <\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/17.png\" alt=\"Clemmensen Reduction\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Wolff Kishner Reduction: Carbonyl group of aldehydes and ketones on treatment with hydrazine  which on heating with sodium hydroxide in a high boiling solvent  (ethylene glycol) reduced to CH<sub>2<\/sub> group. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/18.png\" alt=\"Wolff Kishner Reduction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Tollens\u2019 test: Heating an aldehyde with fresh prepared ammoniacal silver nitrate  solution produces a bright silver mirror due to the formation of silver  metal. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/19.png\" alt=\"Tollens\u2019 test\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Fehling\u2019s test: Fehling\u2019s solution A (aqueous copper sulfate) and Fehling solution B  (alkaline sodium potassium tartrate) are mixed in equal amounts before  the test. A reddish brown precipitate is obtained when an aldehyde is heated with Fehling\u2019s reagent. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/20.png\" alt=\"Fehling\u2019s test\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Aldol reaction: Aldehydes and ketones having one \u03b1-hydrogen undergo a reaction in the  presence of dilute alkali as the catalyst to produce \u03b2-hydroxy  aldehydes or \u03b2-hydroxy ketones.<\/li><\/ol>\n\n\n\n<ol class=\"wp-block-list\"><li> Aldol condensation: Aldol and Ketol lose water to provide \u03b1,\u03b2-unsaturated carbonyl compounds which are aldol condensation products. <\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/21.png\" alt=\"Aldol condensation\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Cross aldol condensation: Aldol condensation is carried out between two different aldehydes and ketones. It gives a mixture of four products if both of them include \u03b1-hydrogen atoms. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/22_1.png\" alt=\"Cross aldol condensation\"\/><\/figure><\/div>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/22_2.png\" alt=\"Cross aldol condensation\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Cannizzaro reaction: Aldehydes without \u03b1-hydrogen atom undergo self-oxidation and reduction reaction when prepared with concentrated alkali. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/23.png\" alt=\"Cannizzaro reaction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Kolbe electrolysis: in Kolbe electrolysis,  An aqueous solution of sodium or potassium salt of a carboxylic acid  gives alkane containing an even number of carbon atoms on electrolysis. <\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/24.png\" alt=\"Kolbe electrolysis\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Hell-Volhard-Zelinsky (HVZ )reaction: Carboxylic acids having an \u03b1-hydrogen are halogenated at the \u03b1-position give \u03b1-halo carboxylic acids on treatment with chlorine or bromine in the presence of a small amount of red phosphorus. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/25.png\" alt=\"Hell-Volhard-Zelinsky (HVZ )reaction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Gabriel phthalimide synthesis: Phthalimide prepared with ethanolic potassium hydroxide produces potassium salt of phthalimide when heated with alkyl halide followed by alkaline hydrolysis forms the corresponding primary amine. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/26.png\" alt=\"Gabriel phthalimide synthesis\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Hoffmann bromamide degradation reaction: An amide with bromine in an aqueous solution of sodium hydroxide produces primary amines. The migration of an alkyl or aryl group takes place from carbonyl carbon of the amide to the nitrogen atom. The amine so produced include one carbon less than that present in the amide. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/27.png\" alt=\"Hoffmann bromamide degradation reaction\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Carbylamine reaction: Aliphatic and aromatic primary amines when heated with chloroform and ethanolic potassium hydroxide produces isocyanides or carbyl amines which are foul-smelling substances. <\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/28.png\" alt=\"Carbylamine reaction\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li> Hinsberg\u2019s Test: Benzenesulfonyl chloride (C<sub>6<\/sub>H<sub>5<\/sub>SO<sub>2<\/sub>Cl) reacts with primary and secondary amines to produce sulphonamides. <ol><li>The reaction of benzene-sulfonyl chloride with primary amine yields  N-ethyl benzene-sulfonyl amide. The hydrogen attached to the nitrogen in sulphonamide is strongly acidic due to the presence of strong electron-withdrawing sulfonyl group. Hence, it is soluble in alkali.<\/li><\/ol><\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/29.png\" alt=\"Hinsberg\u2019s Test\"\/><\/figure><\/div>\n\n\n\n<ol class=\"wp-block-list\"><li>In the reaction with a secondary amine, N, N-diethyl-  benzenesulfonamide is formed. Since N, N- diethyl benzene sulphonamide does not contain any hydrogen atom attached to a nitrogen atom, it is not acidic and hence insoluble in alkali.<br> <ol><li>Tertiary amines do not react with benzene-sulfonyl chloride. <\/li><\/ol><\/li><\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/29_1.png\" alt=\"Hinsberg\u2019s Test\"\/><\/figure><\/div>\n\n\n\n<p><\/p>\n\n\n\n<ol class=\"wp-block-list\"><li> Coupling Reactions: Benzene diazonium chloride gets reacted with phenol in which the phenol molecule at its para-position is mixed with the diazonium salt to give p-hydroxyazobenzene. <\/li><\/ol>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/cdn1.byjus.com\/wp-content\/uploads\/2018\/11\/chemistry\/wp-content\/uploads\/2016\/03\/30.png\" alt=\"Coupling Reactions\"\/><\/figure><\/div>\n\n\n\n<h2 class=\"wp-block-heading\">Chemistry All Reactions  <\/h2>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"\"><tbody><tr><th>Reactions  <\/th><th>DOWNLOADS <\/th><\/tr><tr><td>All reactions <\/td><td><a href=\"http:\/\/sbgstudy.com\/documents\/notes\/class%2012\/chemistry\/chemsitry-all-reactions-sbgstduy.pdf\">Click Here<\/a><\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"http:\/\/www.sbgstudy.com\/blog\/chemistry-class-12\/\">Chemistry important questions <\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Chemistry Class 12 All Chemistry Naming Reactions of Board Exam Here are some important chemical reactions which every student of class 12 must have a thorough understanding of. Sandmeyer Reaction: The Sandmeyer reaction is a chemical reaction that is used to synthesize aryl halides from aryl diazonium salts. This reaction is a method for substitution [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[4],"tags":[],"class_list":["post-638","post","type-post","status-publish","format-standard","hentry","category-class-12"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.6 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Chemistry Class 12 All Chemistry Naming Reactions of Board Exam<\/title>\n<meta name=\"description\" content=\"Chemistry Class 12 All Chemistry Naming Reactions of Board Exam Download Free form sbg study and For scoring good Marks in Chemistry Class 12\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/sbgstudy.in\/blog\/chemistry-naming-reactions\/\" \/>\n<meta property=\"og:locale\" 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