Which of the compounds will react faster in `S_(N)1` reaction with `""^(-)OH` ion?
`CH_(3)-CH_(2)-ClorC_(6)H_(5)-CH_(2)-Cl`

Explanation

To determine which compound will react faster in an SN1 reaction with the hydroxide ion (OH⁻), we need to analyze the stability of the carbocations formed from the two given compounds: CH₃-CH₂-Cl (ethyl chloride) and C₆H₅-CH₂-Cl (benzyl chloride).

### Step-by-Step Solution:

1. **Identify the Compounds**:
- We have two compounds:
- Ethyl chloride: CH₃-CH₂-Cl
- Benzyl chloride: C₆H₅-CH₂-Cl
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