Clemmensen reduction takes place in the presence of
Zn-Hg with HCl
LiAlH4
H2 and Pt as catalyst
Glycol with KOH
The Clemmensen reduction is a chemical reaction that is utilized to reduce ketones or aldehydes to their corresponding hydrocarbons. This reaction plays a crucial role in organic synthesis and is specifically effective with carbonyl compounds that are stable to acidic conditions. It involves the use of metallic zinc (Zn) amalgamated with mercury (Hg) in the presence of concentrated hydrochloric acid (HCl). The reaction mechanism primarily involves the reduction of the carbonyl group (C=O) to a methylene group (CH2) under the reductive environment provided by Zn-Hg/HCl.
In summary, the Clemmensen reduction specifically takes place in the presence of:
Thus, the correct option among the provided choices is Zn-Hg with HCl.
SN1 reaction mechanism takes place by following three steps –
The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group (which generally consists of halide groups or other electron-withdrawing groups) with a nucleophile in a given organic compound.
The mechanism of an electrophilic aromatic substitution reaction contains three main components which are:
The electrophilic substitution reaction mechanism is composed of three steps, which will be discussed more below.