Hydrocarbons (Alkane, Alkene and Alkyne) MCQ Questions & Answers in Organic Chemistry | Chemistry
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251.
Which one of the following alkenes will react faster with $${H_2}$$ under catalytic hydrogenation conditions ?
( $$R=$$ alkyl substituent )
A
B
C
D
Answer :
$${\text{Stability of alkene}} \propto \frac{1}{{{\text{Heat of hydrogenation of alkene}}}}$$
Greater the number of alkyl groups attached to the double bonded carbon atoms, more stable is the alkene. Hence, given alkene follow the following order of stability.
Hence, faster hydrogenation occurs in
252.
Which of the following compounds are antiaromatic
A
(I) and (V)
B
(II) and (V)
C
(I) and (IV)
D
(V) and (VI)
Answer :
(V) and (VI)
For a compound to be aromatic it must have $$\left( {4n + 2} \right)\pi {e^ - }$$ and system should be planar where $$n$$ is an integer. (V) and (VI) both have $$4\,{e^ - }$$ and planar structure. Hence are Antiaromatic.
253.
Acetylenic hydrogens are acidic because
A
sigma electron density of $$C-H$$ bond in acetylene is nearer to carbon which has 50% $$s$$ - character
B
acetylene has only one hydrogen on each carbon
C
acetylene contains least number of hydrogens among the possible hydrocarbons having two carbons
D
acetylene belong to the class of alkynes with molecular formula $${C_n}{H_{2n - 2}}$$
Answer :
sigma electron density of $$C-H$$ bond in acetylene is nearer to carbon which has 50% $$s$$ - character
Acidic character of alkynes can be explained on the basis of $$sp$$ - hybridisation state of the carbon atom in alkynes. We know that an electron in $$s$$ orbital is more tightly held than in a $$P$$ orbital because $$s$$ - electrons are more closer to the nucleus. In $$sp$$ -hybridisation, $$s$$ - character is more 50% as compared to $$s{p^2}$$ - (33%) or $$s{p^3}$$ - (25%) hybrid orbitals. Due to very large $$s$$ - character, the electrons in $$sp$$ - hybrid orbitals are held tightly by the nucleus and are quite electronegative. Consequently, the electron pair of $$H - C \equiv $$ bond gets displaced more towards the carbon atom and help in the release of $${H^ + }\,ions.$$
For a example ethyne react with sodium metal and release the $${H^ + }\,ions.$$
$$CH \equiv CH + Na \to HC \equiv {C^ - }N{a^ + }$$
254.
Which of the following products cannot be obtained in ozonolysis of $$o$$ - xylene ?
A
B
C
D
Answer :
( $$o$$ - xylene ) which on ozonolysis give A, B and C.
255.
The reaction in terms of intermediates and type of reaction is given below. Mark the incorrect option.
A
B
C
D
Answer :
is an example of electrophilic addition reaction.
256.
$$Anti$$ -Markovnikoff addition of $$HBr$$ is not observed in :
257.
Predict the product $$C$$ obtained in the following reaction of butyne-1.
\[C{{H}_{3}}C{{H}_{2}}-C\equiv CH+HCl\to B\xrightarrow{HI}C\]
A
B
C
D
Answer :
Followed by Markownikoff's rule.
258.
The trans-alkenes are formed by the reduction of alkynes with :
A
$${H_2} - Pd/C,\,BaS{O_4}$$
B
$$NaB{H_4}$$
C
$$Na/liq.\,N{H_3}$$
D
$$Sn - HCl$$
Answer :
$$Na/liq.\,N{H_3}$$
259.
The correct IUPAC name of the following alkane is
A
3, 6-diethyl-2-methyloctane
B
5-isopropyl-3-ethyloctane
C
3-ethyl-5-isopropyloctane
D
3-isopropyl-6-ethyloctane
Answer :
3, 6-diethyl-2-methyloctane
A parent chain with larger number of substituents is preferred.
260.
Which of the following types of reaction occur when a reactant has got a double bond ?
(i) Addition
(ii) Photolysis
(iii) Nucleophilic substitution
(iv) Polymerization
A
(i) and (iv)
B
(i) and (ii)
C
(i), (ii) and (iv)
D
(i), (ii), (iii) and (iv)
Answer :
(i) and (iv)
Addition reaction occurs on a double bond.
The compound containing double bonds are also undergo polymerisation. So, the correct option are both (i) and (iv) e.g