An organic compound 'A' `(C_(9)H_(10)O)` when treated with conc. HI undergoes cleavage to yield compounds ‘B’ and ‘C’. ‘B’ gives yellow precipitate with `AgNO_(3)` where as ‘C’ tautomerizes to ‘D’. ‘D’ givespositive iodoform test. ‘A’ could be :

Options

A.
B.
C.
D.

Explanation

To solve the problem, we need to identify the organic compound 'A' (C₉H₁₀O) based on the given reactions and characteristics of the products formed.

### Step-by-Step Solution:

1. **Understanding the Structure of Compound 'A':**
- The molecular formula of compound 'A' is C₉H₁₀O. This suggests that it could be an ether or a compound with a functional group that can undergo cleavage.

2. **Cleavage Reaction with Conc. HI:**
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