Please show the mechanism of the chemical reaction to get from a benzene to a nitrobeneze to  aniline

H NH₂ ཡིནྣཾ ༥ ཨ ཨནྡྷ༥ ༠ ཨི་ཝཱ, ཙ ཨ་ར༩ H NH3+ the acidity of the amine ion drives the reaction to shift toward the conjugate base of the carboxylic acid product. the resulting carboxylic acid ion is a weaker base than an acetate ion. O aldehydes are more reactive toward nucleophiles than ketones. Onucleophilic attack occurs preferentially at the less hindered carbon of the formyl group.

what is the purpose of Dichlorocarbene Addition to an Alkene?

From benzene, organic compunds with 5 carbonw or less and any other inorganic compound you want. Synthesize the derivative for the naphthalene.

Illustrate the complete synthesis of 1,3,5-tribromobenzene from benzene ?

Design the synthesis of the following products starting from toluene. a) m-chlorine benzoic acid b) 2-bromine-4-nitro toluene c) 1-butyl-4-methyl benzene

Question 25 Identify the product of the reaction of an alkene with diazomethane or the Simmons-Smith reagent (ICH,ZnI). O an epoxide O a cyclopropane O an alcohol O a carbene

Hand written solution is not allowed jiger...

Claisen Condensations (Esters) 1. NaOEt EtO 2. H3O+ м Eto Mechanism

Complete the following reactions by filling in the necessary reacents. ? 3,4-diphenyl-1-butene 3, 4- diphenyl butanoic acid