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0.90 gm of an organic compound C(4)H(10)...

`0.90 gm` of an organic compound `C_(4)H_(10)O_(2) (A)` when treated with sodium gives `224 ml` of hydrogen at `NTP`. Compound (A) can be separated into fraction (B) and
(C ), by crystallisation of which the fraction (B) is resolved into isomers (D) and (E ). Write down the structural formula of (A) to (E ) with proper reasoning.

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i. (A) reacts with `Na` to give `H_(2)` and thus it contains `(-OH)` group.
ii. The molecular weight of `(A) (C_(4)H_(10)O_(2))` is `90`. If one `(OH)` group, then
`90 gm(A)` with `Na` gives `11200 ml H_(2)` (i.e, half mole `H_(2))`
`0.90 gm` o f `(A)` gives `(11200xx0.90)/(90)=112ml` of `H_(2)` at `STP`
Since `0.90 Na` gives `224 ml H_(2)` at `STP`, it contians two `(-OH)` groups.
iii. Keeping in view the above facts `(A)` is ,
iv. `(A)` shows optical isomerism of which `(B)` form is optically active having two isomers `(D)` and `(E )`, `(C )` being the inactive form, therefore `(A), (B), (C )`, and `(D)` are:
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Knowledge Check

  • A neutral compound with molecular formula C_(3)H_(8)O evolves H_(2) when treated with sodium metal and gives iodoform test. The compound is

    A
    `(CH_(3))_(2)CHOH`
    B
    `CH_(3)CH_(2)CH_(2)OH`
    C
    `CH_(3)COCH_(3)`
    D
    `CH_(3)CH_(2)CHO`
  • An organic compound with moleular formula, C_(2)H_(6)O_(2) evolves H_(2) when treated with sodium metal and gives two moles of formaldehyde on oxidation with HIO_(4) . The compound is

    A
    Acetic acid
    B
    Methyl acetate
    C
    Ethylene glycol
    D
    Ethyl alcohol
  • 0.44 gm of organic compound C_(x) H_(y) O which occupied 224 ml at NTP and on combustion gave 0.88 gm CO_(2) . The ratio of X to Y in the compound 1s

    A
    `1:1`
    B
    `1:2`
    C
    `1:3`
    D
    `1:4`
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