Friedel crafts Acylation of benzene with Mechanism|Electrophilic aromtic substitution reactions|chemistry

authentic Education Channel Assalam o Alaikum in this lecture i am going to discuss Friedel crafts Acylation of benzene with Mechanism that is the type of Electrophilic aromtic substitution reactions. this lecture is delivered in urdu ,hindi and english.first of all i define Friedel crafts Acylation of benzene with example and then i prove that Friedel crafts Acylation of benzene is the type of Electrophilic aromtic substitution reactions.introduction of acyl group in benzene ring is called acylation. catalyst used in acylation is AlCl3 that is very active catalyst.i then i explain Friedel crafts Acylation of benzene with Mechanism and cover it in urdu hindi and english. Main contents that i have covered :- 1)definition of acylation.what is acylation. 2)what are examples of acylation. 3)what is mechanism of acylation. 4)How acyl group is introduce in benzene ring or in any aromatic compound. 5)why Acylation is consider as electrophilic Aromtic substitution reactions. 6)i explain what is Acylaion,examples of acylation ,mechanism of acylaion in urdu hindi and english. 7)Acylation of benzene Friedel crafts acylation mechanism friedel craft acylation reaction mechanism friedel craft acylation reaction trick acylation example acylation friedel crafts friedel crafts acylation trick fsc acylation mechanism fsc acylation of benzene acylation kya hota hai friedel crafts acylation in hindi acylation mein kaise likha jata hai acylation mechanism benzene acylation meaning acylation reaction mechanism friedel acylation reaction. 8)Acylation mechanism in detail with easy tricks. This lecture is delivered in Urdu/hindi/English. This Chemistry Lecture is for FSC BSC And MSC Students who want to prepare this topic in detail and gain 100% marks. i am going to tell to this channel is especially for chemistry Lectures and speech. i will deliver chemistry lectures in a simple way . in last if you have any question in this lecture then you may also comment your question in last if you entertain this video or you get some knowledge/information then like ,subscribe and share this channel to maximum students . Thanks......................................................... #FriedelcraftsAcylationofbenzenewithMechanism

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Jones Reagent, H2CrO4 Oxidation of Alcohols Reaction Mechanism Chromic Acid|breath analyzer applic

Assalam o Alaikum in this lecture i am going to discuss the reaction mechanism of the Jones Reagent which is used to oxidized primary alcohols into carboxylic acids and secondary alcohols into ketones. The jones reagent is composed of Chromium Trioxide CrO3, H2O, and H2SO4 (Sulfuric acid) which generates chromic acid H2CrO4. Oxidation of primary alcohols first generates an aldehyde which converts to the geminal / gem diol hydrate form which is then oxidized into a carboxylic acid. Tertiary alcohols are resistant to oxidation.This lecture is delivered in Urdu ,Hindi and English. 1° Alcohols are oxidized to carboxylic acids (RCOOH) under harsher reaction conditions: Na2Cr2O7, K2Cr2O7, or CrO3 in the presence of H2O and H2SO4. The mechanism for the oxidation of 1° alcohols to aldehydes parallels the oxidation of 2° alcohols to ketones detailed is discussed in this lecture. Oxidation of a 1o alcohol to a carboxylic acid requires three operations: oxidation first to the aldehyde, reac

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in this lecture i am going to discuss Prepration of benzyne or aryne by the reaction of chlorobenzene with NaNH2 and liquid ammonia.lecture in urdu ,hindi and english. This organic chemistry video tutorial discusses the reaction between chlorobenzene and with NaNH2 sodium amide And liquid ammonia to form aniline which proceeds via the aryne or benzyne intermediate. this reaction consists of two stages and each stage consists of two steps. stage 1 is the cis elimination of HX from vicinal position and formation of benzyne or aryne. stage 1 consists of step 1 and step 2. step 1 of stage 1 is extraction of proton by a base.step 2 of stage 1 is the elimination of halide ion (X) and formation of benzyne or aryne.stage 2 is the cis addition of base to benzyne or aryne. step 1 of stage 2 is the nucleiophilic attack on any triple bonded carbon of benzyne of aryne like -NH2 . step 2 of stage 2 is the the protonation of solvent from NH3 and formation of amino group -NH2 on benzene and

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