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In the following sequence of reactions \(CH_{3}-Br\overset{KCN}{\rightarrow} A \overset{H_{3}O^{+}}{\rightarrow}B\begin{matrix}ether \\\rightarrow \\ LiAH_{4}\end{matrix}C\) the end product (C) is :
Which one is most reactive towards NS1 reaction ?
SN1 reactions involve the formation of carbocations,order of stability of carbocationis 3° > 2° > 1° hence higher the stability of carbocation, more will be the reactivity of the parent alkyl halide. Moreover the tertiary carbocation formed from (c) is stabilized by two phenyl groups.
Trichloroacetaldehyde, CCl3CHO reacts with chlorobenzene in presence of sulphuric acid and produces :
Benzene reacts with CH3Cl in the presence of anhydrous AlCl3 to form:
Which of the following reactions is an example of nucleophilic substitution reaction?
It is a nucleophilic substitution reaction as here stronger nucleophile OH– is replacing weaker nucleophile X–
In a SN2 substitution reaction of the type
\(R-Br+Cl^{-}\overset{DMF}{\rightarrow}R-Cl+Br^{-}\)which one of the following has the highest relative rate ?
When chlorobenzene is reacted with acetyl chloride in the presence of anhydrous AlCl3, the major product formed is
Ethyl alcohol is used as a preservative for chloroform because it:
The product formed by heating iodoform with KOH is :
Reaction of chloroform with KOH in presence of a primary aromatic amine is called :