Compound '$X$' (molecular formula $C_3H_8O$) reacts with acidic potassium dichromate to give product '$Y$' (molecular formula $C_3H_6O$). '$Y$' gives a silver mirror test. When '$Y$' is reacted with aqueous $NH_2CONHNH_2$ and sodium acetate,it gives product '$Z$'. What is the structure of '$Z$'?

  • A
    $CH_3CH_2CH=NNHCONH_2$
  • B
    $CH_3-C(CH_3)=NCONHNH_2$
  • C
    $CH_3-C(CH_3)=NNHCONH_2$
  • D
    $CH_3CH_2CH=NCONHNH_2$

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$(A)$ $CH_3-CH(OH)-C_2H_5$
$(B)$ $CH_3-CH_2-CH_2-OH$
$(C)$ $CH_3-CO-C_2H_5$
$(D)$ $CH_3-COOH$
$(E)$ $CH_3-CH_2-CHO$

The major product formed in the following reaction is:

In the following reaction:
$\text{Carbonyl compound} + MeOH \xleftarrow[HCl]{} \text{acetal}$
The rate of the reaction is the highest for:

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