`C_(7)H_(14)` (A) decolourises `Br_(2)` in `C CI_(4)` and reacts with `Hg(OAc)_(2)` in THF `H_(2)O` following by reduction with `NaBH_(4)` to produce a resolvable compounds (B). (A) undergoes reductive ozonolysis to give the same compound (C) obtained by oxidation of hexan-3-ol with `KMnO_(4)` . Identify (A), (B), and (C).

Explanation

To solve the problem, we need to identify the compounds A, B, and C based on the given reactions and information.

### Step 1: Identify Compound A
Given the molecular formula \( C_7H_{14} \), we can deduce that it is an alkene since the general formula for alkenes is \( C_nH_{2n} \).

**Hint:** Look for a structure that has a double bond and satisfies the formula \( C_7H_{14} \).

### Step 2: Determine the Structure of A
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