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896 mL vapour of a hydrocarbon ‘A’ having carbon 87.80% and hydrogen 12.19% weighs 3.28 g at STP. Hydrogenation of ‘A’ gives 2-methylpentane. Also ‘A’ on hydration in the presence - Chemistry

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Question

896 mL vapour of a hydrocarbon ‘A’ having carbon 87.80% and hydrogen 12.19% weighs 3.28 g at STP. Hydrogenation of ‘A’ gives 2-methylpentane. Also ‘A’ on hydration in the presence of H2SO4 and HgSO4 gives a ketone ‘B’ having molecular formula C6H12O. The ketone ‘B’ gives a positive iodoform test. Find the structure of ‘A’ and give the reactions involved.

Long Answer

Solution

Step I

896 mL vapour of CxHy (A) weighs 3.28 g

22700 mL vapour of CxHy (A) weighs `(3.28 xx 22700)/896` g mol–1 = 83.1 g mol–1 

Step II

Element Percentage Atom
mass
Relative ratio Relative no.
of atoms
Simplest
ratio
C 87.8% 12 7.31 1 3
H 12.19% 1 12.19 1.66 4.98 

Empirical formula of 'A'C3H5

Empirical formula mass = 35 + 5 = 41 u

n = `"Molecular mass"/"Empirical formula mass" = 83.1/41` = 2.02 ≈ 2

⇒ Molecular mass is double of the empirical formula mass.

∴ Molecular Formula is C6H10

Step III

\[\ce{\underset{(A)}{C6H10} ->[2H2] 2-methylpentane}\]

Structure of 2-methylpentane is

\[\begin{array}{cc}
\ce{CH3}\phantom{...................}\\
\backslash\phantom{..............}\\
\phantom{............}\ce{CH - CH2 - CH2 - CH3}\\
/\phantom{.............}\\
\ce{CH3}\phantom{...................}
\end{array}\]

Hence, the molecule has a five carbon chain with a methyl group at the second carbon atom.

'A' adds a molecule of H2O in the presence of Hg2+ and H+, it should be an alkyne. Two possible structures for 'A' are:

\[\begin{array}{cc}
\ce{CH3}\phantom{...................}\\
\backslash\phantom{..............}\\
\phantom{.......}\ce{CH - C ≡ C - CH3}\\
/\phantom{..............}\\
\ce{CH3}\phantom{...................}
\end{array}\]
I

or

\[\begin{array}{cc}
\ce{CH3}\phantom{...................}\\
\backslash\phantom{..............}\\
\phantom{.........}\ce{CH - CH2 - C ≡ CH}\\
/\phantom{..............}\\
\ce{CH3}\phantom{...................}
\end{array}\]
II

Since the ketone (B) gives a positive iodoform test, it should contain a – COCH3 group. Hence the structure of ketone is as follows:

\[\begin{array}{cc}
\ce{CH3}\phantom{...................}\\
\backslash\phantom{..............}\\
\phantom{...........}\ce{CH - CH2 - CO - CH3}\\
/\phantom{..............}\\
\ce{CH3}\phantom{...................}
\end{array}\]

Therefore structure of alkyne is II.

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Alkanes - Preparation of Alkanes from Unsaturated Hydrocarbons, Alkyl Halides and Carboxylic Acids
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Chapter 13: Hydrocarbons - Multiple Choice Questions (Type - I) [Page 170]

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NCERT Exemplar Chemistry [English] Class 11
Chapter 13 Hydrocarbons
Multiple Choice Questions (Type - I) | Q 49 | Page 170
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