NCERT · Class 12 · Chemistry · Haloalkanes and HaloarenesWhich of the following undergoes $SN1$ reaction most readily?
Step-by-Step Solution
Tert-butyl chloride undergoes $S_N1$ reaction most readily because it forms a tertiary carbocation, which is highly stable due to hyperconjugation and inductive effects.
Detailed Options Breakdown
Option : CH3CH2Cl
Incorrect choice. This distractor represents a common misunderstanding of the core principles of Haloalkanes and Haloarenes.
Option 1: (CH3)2CHCl
Incorrect choice. This distractor represents a common misunderstanding of the core principles of Haloalkanes and Haloarenes.
Option 2: (CH3)3CCl (Correct Answer)
Correct choice. Refer to the step-by-step verified solution guidelines above for details.
Option 3: CH3Cl
Incorrect choice. This distractor represents a common misunderstanding of the core principles of Haloalkanes and Haloarenes.
💡 Study Guide: This question tests core syllabus concepts from Haloalkanes and Haloarenes. For formulas, key summaries, and mock exam reference guides, read the full Haloalkanes and Haloarenes Revision Notes.