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NEET • CHEMISTRY • HYDROCARBONS

Hydrocarbons practice · Mixed difficulty

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Showing 1-30 of 229 questions
1 Easy
1 of 229
Remembering +4 | -1
The reaction of alkanes with halogen is explosive in the case of:
View answer and explanation
Correct option: A
F2{\mathrm{F}_2}
Option A (F2{\mathrm{F}_2}) is correct because the reaction of alkanes with fluorine is highly exothermic and explosive.
2 Easy
2 of 229
Understanding +4 | -1
A mixture of sodium benzoate and soda lime on heating produces
View answer and explanation
Correct option: B
C6H6{C_6}{H_6}
Option B (C6H6{C_6}{H_6}) is correct because sodium benzoate and soda lime on heating undergo decarboxylation to form benzene.
3 Hard
3 of 229
Application +4 | -1
The major product of the following reaction is CH3C≡CH→(ii)  DI(i)  DCl  (1  equiv.)C{H_3}C \equiv CH\xrightarrow[{(ii)\;DI}]{{(i)\;DCl\;(1\;equiv.)}}
View answer and explanation
Correct option: D
CH3C(I)(Cl)CHD2C{H_3}C(I)(Cl)CH{D_2}
The correct answer is CH3C(I)(Cl)CHD2C{H_3}C(I)(Cl)CH{D_2} because DCl adds first according to Markovnikov's rule, followed by DI.
4 Hard
4 of 229
Analyzing +4 | -1
S-I : Heavy metal acetylides can be used to purify alkynes
S-II: Terminal alkynes form acetylides which are soluble in acids.
View answer and explanation
Correct option: A
S-I &\& S-II are true
Option A is correct because heavy metal acetylides are used to purify alkynes by selectively precipitating them, and terminal alkynes do form acetylides that are soluble in acids, allowing for their regeneration.
5 Medium
5 of 229
Analyzing +4 | -1
Select the incorrect statement regarding A
CH3−C≡CH+H2OAC{H_3} - C \equiv CH + {H_2}OA
View answer and explanation
Correct option: D
Reduces Tollen’s reagent
Option D is correct because the product A, which is 2-propanone (acetone), does not reduce Tollen's reagent. Ketones generally do not reduce Tollen's reagent, while aldehydes do.
6 Medium
6 of 229
Remembering +4 | -1
Kharasch effect is based on
View answer and explanation
Correct option: A
Free radical addition
Option A (Free radical addition) is correct because the Kharasch effect, also known as the peroxide effect, involves a free radical addition mechanism.
7 Medium
7 of 229
Analyzing +4 | -1
A compound X(C5H8)X\left( {{\mathrm{C}_5}{\mathrm{H}_8}} \right) reacts with ammoniacal AgNO3\mathrm{AgN}{\mathrm{O}_3} to give a white precipitate, and on oxidation with hot alkaline KMnO4\mathrm{KMn}{\mathrm{O}_4} gives the acid,(CH3)2CHCOOH{\left( {\mathrm{C}{\mathrm{H}_3}} \right)_2}\mathrm{CHCOOH}. Therefore, XX is
View answer and explanation
Correct option: C
(CH3)2CH−C≡CH{\left( {\mathrm{C}{\mathrm{H}_3}} \right)_2}\mathrm{CH} - \mathrm{C} \equiv \mathrm{CH}
Option C is correct because the compound X reacts with ammoniacal silver nitrate to give a white precipitate, indicating it is a terminal alkyne. Upon oxidation, it yields isobutyric acid, which confirms the structure of X as 3-methyl-1-butyne.
8 Easy
8 of 229
Understanding +4 | -1
The reactivity of halogens towards any given alkane is in order of
View answer and explanation
Correct option: B
F2>Cl2>Br2>I2{F_2} > C{l_2} > B{r_2} > {I_2}
Option B (F2>Cl2>Br2>I2{F_2} > C{l_2} > B{r_2} > {I_2}) is correct because the reactivity of halogens towards alkanes decreases down the group due to decreasing bond dissociation energy.
9 Hard
9 of 229
Understanding +4 | -1
The gas ′A′'A' is having very low reactivity reaches to stratosphere. It is non-toxic and non-flammable but dissociated by UV—radiations in stratosphere. The intermediates formed initially from the gas ′A′'A' are
View answer and explanation
Correct option: D
C∙l+CF2∙Cl\mathop \mathrm{C}\limits^ \bullet \mathrm{l + C}\mathop {{\mathrm{F}_2}}\limits^ \bullet \mathrm{Cl}
Option D (C∙l+CF2∙Cl\mathop \mathrm{C}\limits^ \bullet \mathrm{l + C}\mathop {{{{F}}_2}}\limits^ \bullet \mathrm{Cl}) is correct because the gas 'A' is a CFC (Chlorofluorocarbon), which upon UV radiation dissociates into chlorine free radical and a fluorocarbon free radical.
10 Easy
10 of 229
Application +4 | -1
The treatment of benzene with benzoyl chloride in the presence of AlCl3\mathrm{AlC}{\mathrm{l}_3} gives
View answer and explanation
Correct option: B
Benzophenone
Benzophenone is the correct answer because the reaction of benzene with benzoyl chloride in the presence of AlCl3\mathrm{AlC}{\mathrm{l}_3} is a Friedel-Crafts acylation, which adds a benzoyl group to benzene.
11 Easy
11 of 229
Application +4 | -1
Electrolysis of cold concentrated aqueous solution of potassium succinate yields
View answer and explanation
Correct option: C
ethene
Option C (ethene) is correct because the electrolysis of potassium succinate leads to the formation of ethene via the Kolbe electrolysis mechanism.
12 Easy
12 of 229
Application +4 | -1
Isopropyl bromide on Wurtz reaction gives
View answer and explanation
Correct option: C
2,3-dimethyl butane
Option C (2,3-dimethyl butane) is correct because the Wurtz reaction involves coupling two alkyl halides, and in this case, two isopropyl groups combine to form 2,3-dimethylbutane.
13 Easy
13 of 229
Understanding +4 | -1
Anti-addition of hydrogen atoms to the triple bond takes place by
View answer and explanation
Correct option: B
Li/NH3Li/N{H_3}
Option B (Li/NH3Li/N{H_3}) is correct because the reduction of alkynes with lithium in liquid ammonia results in trans-addition of hydrogen atoms.
14 Hard
14 of 229
Analyzing +4 | -1
The isomer of C6H14,\mathrm{C}_6 \mathrm{H}_{14}, which will give maximum number of monochloroderivative is
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Correct option: B
2-methylpentane
Option B (2-methylpentane) is correct because it has the most non-equivalent hydrogen atoms, leading to the maximum number of monochloro derivatives.
15 Medium
15 of 229
Understanding +4 | -1
Alkene-1 on hydroboration followed with action of H2O2{\mathrm{H}_2}{\mathrm{O}_2} gives:
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Correct option: B
Alkanol-1
Option B (Alkanol-1) is correct because hydroboration-oxidation of an alkene results in anti-Markovnikov addition of water, leading to the formation of a primary alcohol (alkanol-1).
16 Medium
16 of 229
Understanding +4 | -1
Which of the following reagent is not involved in the halogenation of benzene
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Correct option: C
Br2/CCl4B{r_2}/CC{l_4}
Option C (Br2/CCl4B{r_2}/CC{l_4}) is correct because Br2/CCl4B{r_2}/CC{l_4} is used for the addition reaction with alkenes, not for the halogenation of benzene.
17 Easy
17 of 229
Analyzing +4 | -1
Which of the following compounds contain 10,20,30{1^0},{2^0},{3^0} as well as 40{4^0} carbon atoms
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Correct option: D
2,2,3-trimethyl pentane
Option D (2,2,3-trimethyl pentane) is correct because it contains primary, secondary, tertiary, and quaternary carbon atoms.
18 Medium
18 of 229
Application +4 | -1
What volume of CH4\mathrm{C}{\mathrm{H}_4} at NTP is formed when 20.5 g of CH3COONa\mathrm{C}{\mathrm{H}_3}\mathrm{COONa} a is treated with sodalime?
View answer and explanation
Correct option: D
5.6 litre
Option D (5.6 litre) is correct because 20.5 g of CH3COONa produces 0.25 moles of methane, which occupies 5.6 liters at NTP.
19 Easy
19 of 229
Analyzing +4 | -1
An alkene on vigorous oxidation with KMnO4\mathrm{KMn}{\mathrm{O}_4} gives only acetic acid. The alkene is
View answer and explanation
Correct option: B
CH3CH=CHCH3\mathrm{C}{\mathrm{H}_3}\mathrm{CH} = \mathrm{CHC}{\mathrm{H}_3}
Option B (CH3CH=CHCH3\mathrm{C}{\mathrm{H}_3}\mathrm{CH} = \mathrm{CHC}{\mathrm{H}_3}) is correct because vigorous oxidation with KMnO4\mathrm{KMn}{\mathrm{O}_4} yields only acetic acid.
20 Easy
20 of 229
Understanding +4 | -1
Which one of the following is not an oxidation product of alkane
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Correct option: D
ether
Option D (ether) is correct because ethers are not direct oxidation products of alkanes. Oxidation of alkanes typically yields alcohols, aldehydes, and carboxylic acids.
21 Hard
21 of 229
Understanding +4 | -1
The Baeyer angle strain is minimum in
View answer and explanation
Correct option: C
Cyclopentane
Option D (Cyclohexane) is correct because cyclohexane exists in a chair conformation, which minimizes angle strain, making it the most stable cycloalkane among the given options.
22 Medium
22 of 229
Remembering +4 | -1
On passing benzene vapour through a tube at 700−800∘C700 - 800^\circ C or through molten lead we get:
View answer and explanation
Correct option: A
Diphenyl
Option A (Diphenyl) is correct because passing benzene vapor through a hot tube or molten lead causes dimerization to form diphenyl.
23 Medium
23 of 229
Analyzing +4 | -1
Which among the following is very strong o−, p−o - ,\,p - directing group?
View answer and explanation
Correct option: D
−NHR- \mathrm{NHR}
Option D (−NHR-\mathrm{NHR}) is correct because alkylated amines are stronger activating groups than alcohols, halides, or unsubstituted amines due to increased electron donation.
24 Medium
24 of 229
Analyzing +4 | -1
When CaC2\mathrm{Ca}{\mathrm{C}_2} was hydrolysed a gas was obtained. It had a garlic odour due to phosgene present as impurity. The gas was passed through ammoniacal solution of Cu2Cl2\mathrm{C}{\mathrm{u}_2}\mathrm{C}{\mathrm{l}_2}, ared ppt. was obtained. The gas was:
View answer and explanation
Correct option: C
Acetylene
Option C is correct because acetylene (ethyne) reacts with cuprous chloride in an ammoniacal solution to form a red precipitate of copper acetylide. The garlic odor is due to phosphine impurity in the calcium carbide.
25 Easy
25 of 229
Application +4 | -1
Major product of the following reaction is
CH3CH2CCl∣HCH3→ΔAlC.KOHC{H_3}C{H_2}\mathop C\limits_{\mathop {Cl}\limits^| } HC{H_3}\xrightarrow[\Delta ]{{AlC.KOH}}
View answer and explanation
Correct option: B
but-2-ene
Option B (but-2-ene) is correct because the major product of the dehydrohalogenation reaction is the more substituted alkene (Zaitsev's rule).
26 Hard
26 of 229
Application +4 | -1
At constant temperature and pressure, the percentage of butane by volume in a mixture of butane, propane and propyne is 40%.40 \%. What will be the volume of CO2(g)\mathrm{CO}_{2(\mathrm{g})} (in ml) under same pressure and temperature produced, when 150 ml of gaseous mixture is burnt in excess of O2?\mathrm{O}_2?
View answer and explanation
Correct option: C
510 ml
Option C (510 ml) is correct because it is calculated based on the combustion equations of butane, propane, and propyne, considering the given percentage of butane.
27 Hard
27 of 229
Analyzing +4 | -1
Which is the most suitable reagent among the following to distinguish compound (3) from rest of the compounds?
i)    CH3−C≡C−CH3\mathrm{i)}\,\,\,\,C{H_3} - C \equiv C - C{H_3}
ii)    CH3−CH2−CH2−CH3\mathrm{ii)}\,\,\,\,C{H_3} - C{H_2} - C{H_2} - C{H_3}
iii)    CH3−CH2C≡CH\mathrm{iii)}\,\,\,\,C{H_3} - C{H_2}C \equiv CH
iv)    CH3−CH=CH2.\mathrm{iv)}\,\,\,\,C{H_3} - CH = C{H_2}.
View answer and explanation
Correct option: D
Ammonical silver nitrate
Option D is correct because ammoniacal silver nitrate reacts specifically with terminal alkynes (like compound iii) to form a precipitate, while it does not react with internal alkynes, alkanes, or alkenes.
28 Medium
28 of 229
Analyzing +4 | -1
Which of the following will not produce ethane?
View answer and explanation
Correct option: B
Reduction of CH3COCH3\mathrm{C}{\mathrm{H}_3}\mathrm{COC}{\mathrm{H}_3} with HI and red P
Option B (Reduction of CH3COCH3\mathrm{C}{\mathrm{H}_3}\mathrm{COC}{\mathrm{H}_3} with HI and red P) is correct because the reduction of acetone (propanone) with HI and red P yields propane, not ethane.
29 Medium
29 of 229
Application +4 | -1
In the reaction sequence, the product YY is
C6H6→AlCl3CH3ClX→KMnO4Y{C_6}{H_6}\xrightarrow[{AlC{l_3}}]{{C{H_3}Cl}}X\xrightarrow{{KMn{O_4}}}Y
View answer and explanation
Correct option: C
benzoic acid
Option A is correct because the reaction requires deprotonation of both acidic hydrogens of ethyne using NaNH2NaNH_2, followed by alkylation with excess ethyl iodide to form Hex-3-yne.
30 Hard
30 of 229
Analyzing +4 | -1
(A): 1-butene on reaction with HBr\mathrm{HBr} in the presence of a peroxide, produces 1-bromobutane
(R): It involves the formation of a primary radical.
View answer and explanation
Correct option: C
A is true, but R is false
Option C (A is true, but R is false) is correct because 1-butene reacts with HBr in the presence of a peroxide to produce 1-bromobutane (anti-Markovnikov addition), but this occurs via a secondary radical intermediate, not a primary radical.
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