Structure and synthesis of nucleophilic substitution reaction
Answers
Answer:
nucleophilic substitution reactions invove halogenoalkane
Explanation:
substitution with NaOH aq gives an alcohol
the nucleophile is OH- ion.
reaction with CH3CH2Br gives CH3CH2OH and NaBr
substitution with KCN along with ethanol gives a nitrile
the nucleophile is CN-
reaction with CH3CH2Br gives CH3CH2CN and KBr
substitution with ammonia along with ethanol gives a nitrile
nuclephile is NH3
reaction with CH3CH2Br gives CH3CH2NH2
if CH3CH2Br is in excess there is secondary amine [CH3CH2]2 NH
tertiary amine and so on
Explanation:
The most general form of the reaction may be given as the following: Nuc: + R-LG → R-Nuc + LG: The electron pair (:) from the nucleophile (Nuc) attacks the substrate (R-LG) and bonds with it. ... Nucleophilic substitution reactions are common in organic chemistry (especially introductory organic chemistry