Account for the following:
t-butyl chloride on heating with sodium methoxide gives 2-methylpropene instead of t-butylmethylether

Explanation

To account for why t-butyl chloride on heating with sodium methoxide gives 2-methylpropene instead of t-butyl methyl ether, we can break down the reaction mechanism step by step.

### Step 1: Understand the Reactants
- **Tert-butyl chloride (t-butyl chloride)** is a tertiary alkyl halide with the formula (CH₃)₃CCl.
- **Sodium methoxide (NaOCH₃)** is a strong nucleophile and base.

### Step 2: Analyze the Reaction Conditions
- When t-butyl chloride is heated with sodium methoxide, the reaction conditions favor elimination rather than substitution. Heating typically promotes elimination reactions.
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