The reactivity of alkyl bromides towards iodide ion in dry acetone decreases in the order:
$I. CH_3CH_2Br$
$II. CH_3-CH(CH_3)-Br$
$III. CH_3-C(CH_3)_2-Br$
$IV. CH_3Br$
$I. CH_3CH_2Br$
$II. CH_3-CH(CH_3)-Br$
$III. CH_3-C(CH_3)_2-Br$
$IV. CH_3Br$
- A$IV > I > II > III$
- B$I > IV > II > III$
- C$III > II > I > IV$
- D$III > II > IV > I$
Explore More
Similar Questions
Identify the products $A$ and $B$ in the reactions :
$R-X + AgCN \longrightarrow A + AgX$
$R-X + KCN \longrightarrow B + KX$
$R-X + AgCN \longrightarrow A + AgX$
$R-X + KCN \longrightarrow B + KX$
MediumKCET 2022
View SolutionWhich of the following is an incorrect statement?
Medium
View Solution$C_2H_5I$ $\xrightarrow{\text{alc. } KOH} X$ $\xrightarrow{Br_2} Y$ $\xrightarrow{KCN} Z$; $Z = \dots$
Medium
View SolutionWhich of the following compounds will undergo $E_2$ elimination reaction to give a single product in the presence of a strong base?
Difficult
View SolutionWhich of the following reactions is an example of a nucleophilic substitution reaction?
Medium
View SolutionVedclass Products
For Students
Vedclass Test Series
Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.
Start Free TrialFor Teachers
Exam Paper Generator
Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.
Try FreeFor Institutes
Online Exam Module
Live online exams with unlimited students, 360° analytics & white-label branding.
See Demo