JEE Chemistry Hydrocarbons MCQs Set C

Refer to JEE Chemistry Hydrocarbons MCQs Set C provided below available for download in Pdf. The MCQ Questions for Full Syllabus Chemistry with answers are aligned as per the latest syllabus and exam pattern suggested by JEE (Main), NCERT and KVS. Multiple Choice Questions for Hydrocarbons are an important part of exams for Full Syllabus Chemistry and if practiced properly can help you to improve your understanding and get higher marks. Refer to more Chapter-wise MCQs for JEE (Main) Full Syllabus Chemistry and also download more latest study material for all subjects

MCQ for Full Syllabus Chemistry Hydrocarbons

Full Syllabus Chemistry students should refer to the following multiple-choice questions with answers for Hydrocarbons in Full Syllabus.

Hydrocarbons MCQ Questions Full Syllabus Chemistry with Answers

 

 

Question:

  • a) A – (r), B – (p), C – (s), D – (q)
  • b) A – (p), B – (s), C – (r), D – (q)
  • c) A – (s), B – (q), C – (p), D – (r)
  • d) A – (q), B – (p), C – (s), D – (r)

Answer: A – (r), B – (p), C – (s), D – (q)

 

Question:

  • a) A – (r), B – (p), C – (s), D – (q)
  • b) A – (p), B – (q), C – (r), D – (s)
  • c) A – (q), B – (p), C – (s), D – (r)
  • d) A – (s), B – (p), C – (r), D – (s)

Answer: A – (r), B – (p), C – (s), D – (q)

 

Question:

  • a) A – (r), B – (s), C – (p), D – (q)
  • b) A – (s), B – (r), C – (q), D – (p)
  • c) A – (q), B – (p), C – (s), D – (r)
  • d) A – (r), B – (s), C – (q), D – (p)

Answer: A – (r), B – (s), C – (p), D – (q)

 

Question:

  • a) A – (q), B – (r), C – (s), D – (p)
  • b) A – (s), B – (r), C – (q), D – (p)
  • c) A – (r), B – (p), C – (q), D – (s)
  • d) A – (q), B – (p), C – (s), D – (r)

Answer: A – (q), B – (r), C – (s), D – (p)

 

Question:

  • a) A – (s), B – (r), C – (q), D – (p)
  • b) A – (s), B – (r), C – (p), D – (q)
  • c) A – (r), B – (s), C – (p), D – (q)
  • d) A – (r), B – (s), C – (q), D – (p)

Answer: A – (s), B – (r), C – (q), D – (p)

 

Question:

  • a) A - (q), B - (s), C - (p); D - (r)
  • b) A - (r), B - (p), C - (s); D - (q)
  • c) A - (s), B - (q), C - (r); D - (p)
  • d) A - (p), B - (r), C - (q); D - (s)

Answer: A - (q), B - (s), C - (p); D - (r)

 

Question:

  • a) A - (p, s), B - (p, r), C - (s), D - (q, r)
  • b) A - (p, r), B - (p, s), C - (s), D - (q, r)
  • c) A - (p, s), B - (s), C - (p, r), D - (q, r)
  • d) A - (q, r), B - (p, r), C - (s), D - (p, s)

Answer: A - (p, s), B - (p, r), C - (s), D - (q, r)

 

Question:

  • a) A – (s), B – (p, r), C – (q, r), D – (r)
  • b) A – (r), B – (p, r), C – (q, r), D – (s)
  • c) A – (p, r), B – (s), C – (q, r), D – (r)
  • d) A – (s), B – (p, r), C – (r), D – (q, r)

Answer: A – (s), B – (p, r), C – (q, r), D – (r)

 

Question:

Statement-1 : 1-Butene on reaction with HBr in the presence of a peroxide produces 1-bromobutane.
Statement-2 : It involves the free radical mechanism.

  • a) Assertion is correct, reason is correct; reason is a correct explanation for assertion
  • b) Assertion is correct, reason is correct; reason is not a correct explanation for assertion
  • c) Assertion is correct, reason is incorrect
  • d) Assertion is incorrect, reason is correct

Answer: Assertion is correct, reason is correct; reason is a correct explanation for assertion

 

Question:

Statement-1 : Iodination of alkanes is reversible.
Statement-2 : Iodination is carried out in presence of iodic acid.

  • a) Assertion is correct, reason is correct; reason is not a correct explanation for assertion
  • b) Assertion is correct, reason is correct; reason is a correct explanation for assertion
  • c) Assertion is correct, reason is incorrect
  • d) Assertion is incorrect, reason is correct

Answer: Assertion is correct, reason is correct; reason is not a correct explanation for assertion

 

Question:

Statement-1 : CH4 does not react with Cl2 in dark.
Statement-2 : Chlorination of CH4 takes place in sunlight.

  • a) Assertion is correct, reason is correct; reason is not a correct explanation for assertion
  • b) Assertion is correct, reason is correct; reason is a correct explanation for assertion
  • c) Assertion is correct, reason is incorrect
  • d) Assertion is incorrect, reason is correct

Answer: Assertion is correct, reason is correct; reason is not a correct explanation for assertion

 

Question:

Statement-1 : All the hydrogen atoms in CH2 = C = CH2 lie in one plane.
Statement-2 : Carbon atoms are sp2 and sp hybridized

  • a) Assertion is incorrect, reason is correct.
  • b) Assertion is correct, reason is correct; reason is a correct explanation for assertion
  • c) None of these
  • d) Assertion is incorrect, reason is correct

Answer: Assertion is incorrect, reason is correct.

 

Question:

  • a) Assertion is correct, reason is incorrect
  • b) Assertion is incorrect, reason is correct
  • c) Assertion is correct, reason is correct; reason is not a orrect explanation for assertion
  • d) Assertion is correct, reason is correct; reason is a correct explanation for assertion

Answer: Assertion is correct, reason is incorrect

 

Question: In cyclopropane, cyclobutane and cyclohexane, the common group is

  • a)

  • b)

  • c)

  • d)

Answer:

 

Question: The number of primary, secondary, tertiary and quaternary carbons in neopentane are respectively

  • a) 4, 0, 0 and 1
  • b) 4, 3, 2 and 1
  • c) 5, 0, 0 and 1
  • d) 4, 0, 1 and 1

Answer: 4, 0, 0 and 1

 

More Questions.........................................

 

Question:

  • a) 3, 4, 4–Trimethyl octane
  • b) 3, 4, 4–Trimethyl heptane
  • c) 2–Ethyl, 3,3–dimethyl heptane
  • d) 2–Butyl, 2 methyl,3–ethyl butane

Answer: 3, 4, 4–Trimethyl octane

 

Question: Which one of the following has the lowest boiling point?

  • a) 2-methyl propane
  • b) 2-methylbutane
  • c) 2, 2-dimethyl propane
  • d) n-pentane

Answer: 2-methyl propane

 

Question:  Arrange the following in decreasing order of their boiling points.

(A) n–butane   (B) 2-methylbutane
(C) n-pentane  (D) 2, 2–dimethylpropane

  • a) C > B > D > A
  • b) B > C > D > A
  • c) A > B > C > D
  • d) D > C > B > A

Answer: C > B > D > A

 

Question: When neo-pentyl bromide is subjected to Wurtz reaction, the product formed is

  • a) 2,2,5,5-tetramethylhexane
  • b) 2,2,3,3-tetramethylhexane
  • c) 2,2,4,4-tetramethylpentane
  • d) 2,2,4,4-tetramethylhexane

Answer: 2,2,5,5-tetramethylhexane

 

Question: Which one of the following reactions is expected to readily give a hydrocarbon product in good yields ?

  • a)

  • b)

  • c)

  • d)

Answer:

 

Question: A hydrocarbon A on chlorination gives B which on heating with alcoholic potassium hydroxide changes into another hydrocarbon C. The latter decolourises Baeyer's reagent and on ozonolysis forms formaldehyde only. A is

  • a) Ethane
  • b) Butane
  • c) Ethene
  • d) Methane

Answer: Ethane

 

Question: Which of the following compounds can yield only one monochlorinated product upon free radical chlorination?

  • a) 2, 2-Dimethylpropane
  • b) n-Butane
  • c) Propane
  • d) 2-Methylpropane

Answer: 2, 2-Dimethylpropane

 

Question:

  • a) the molecular plane
  • b) a plane parallel to the molecular plane
  • c) Both
  • d) None of these

Answer: the molecular plane

 

Question: The IUPAC name of the compound having the formula (CH3)3CCH = CH2 is –

  • a) 3, 3-dimethyl-1-butene
  • b) 1, 1, 1-trimethyl-1-butene
  • c) 3, 3, 3-trimethyl-1-propane
  • d) None of these

Answer: 3, 3-dimethyl-1-butene

 

Question:

  • a) trans-2-chloro-3-iodo-2-pentene
  • b) cis-3-iodo-4-chloro-3-pentene
  • c) trans-3-iodo-4-chloro-3-pentene
  • d) cis-2-chloro-3-iodo-2-pentene

Answer: trans-2-chloro-3-iodo-2-pentene

 

Question: The number of possible open chain (acyclic) isomeric compounds for molecular formula C5H10 would be

  • a) 6
  • b) 8
  • c) 7
  • d) 5

Answer: 6

 

Question: Correct order of stability is

  • a) trans-2-butene > cis-2-butene > 1-butene
  • b) 1-butene > cis-2-butene > trans-2- butene
  • c) cis-2-butene > trans-2-butene > 1-butene
  • d) cis -2- butene > 1-butene > trans -2-butene

Answer: trans-2-butene > cis-2-butene > 1-butene

 

Question: But-2-ene exhibits cis-trans-isomerism due to

  • a) restricted rotation around C = C bond
  • b) rotation around C3 – C4 sigma bond
  • c) rotation around C1 – C2 bond
  • d) None of these

Answer: restricted rotation around C = C bond

 

Question:

  • a)

  • b)

  • c)

  • d) None of these

Answer:

 

Question: Aromatisation of n-hexane gives

  • a) benzene
  • b) toluene
  • c) cyclohexane
  • d) cycloheptane

Answer: benzene

 

Question: When 3, 3-dimethyl 2-butanol is heated with H2SO4, the major product obtained is

  • a) 2,3-dimethyl 2-butene
  • b) 3, 3-dimethyl 1- butene
  • c) 2, 3-dimethyl 1- butene
  • d) cis & trans isomers of 2, 3-dimethyl 2-butene

Answer: 2,3-dimethyl 2-butene

 

Question:

  • a) 2, 3-dimethyl-2-pentene
  • b) 3, 4-dimethyl-2-pentene
  • c) 3, 4-dimethyl-3-pentene
  • d) 2, 3-dimethyl-3-pentene

Answer: 2, 3-dimethyl-2-pentene

 

Question: Reaction of hydrogen bromide with propene in the absence of peroxide is a/an

  • a) electrophilic addition
  • b) electrophilic substitution
  • c) nucleophilic addition
  • d) free radical addition

Answer: electrophilic addition

 

Question: 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) (iii) and (iv)
  • c) (i), (ii) and (iii)
  • d) (ii) and (iii)

Answer: (i) and (iv)

 

Question: The disappearance of the characteristic purple colour of KMnO4 in its reaction with an alkene is the test for unsaturation. It is known as

  • a) Baeyer test
  • b) Grignard test
  • c) Markownikoff test
  • d) Wurtz test

Answer: Baeyer test

 

Question:  CH2 = CHCl reacts with HCl to form

  • a)

  • b)

  • c)

  • d) None of these

Answer:

 

Question: The only alcohol that can be prepared by the indirect hydration of alkene is

  • a) Ethyl alcohol
  • b) Propyl alcohol
  • c) Isobutyl alcohol
  • d) Methyl alcohol

Answer: Ethyl alcohol

 

Question: Which reactions are most common in alkenes

  • a) Electrophilic addition reactions
  • b) Nucleophilic addition reactions
  • c) Nucleophillic substitution reactions
  • d) Electrophilic substitution reactions

Answer: Electrophilic addition reactions

 

Question: In the presence of peroxide, hydrogen chloride and hydrogen iodide do not give anti-Markownikov’s addition to alkenes because

  • a) One of the steps is endothermic in both the cases
  • b) All the steps are exothermic in both the cases
  • c) One is oxidising and the other is reducing
  • d) Both are highly ionic

Answer: One of the steps is endothermic in both the cases

 

Question: Which of the following statements is incorrect regarding dehydrohalogenation of alkenes ?

  • a) Only nature of halogen atom determine rate of the reaction
  • b) Rate of reaction for same alkyl group; Iodine > Bromine > Chlorine
  • c) Both
  • d) None of these

Answer: Only nature of halogen atom determine rate of the reaction

 

Question: How many structural isomers are possible for the alkyne C6H10 ?

  • a) 7
  • b) 8
  • c) 6
  • d) 5

Answer: 7

 

Question: Which of the following will have least hindered rotation around carbon - carbon bond ?

  • a) Ethane
  • b) Acetylene
  • c) Ethylene
  • d) Hexachloroethane

Answer: Ethane

 

Question: 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 open hydrogen in each carbon
  • c) Acetylene contains least number of hydrogens among the possible hydrocarbons having two carbons
  • d) None of these

Answer: Sigma electron density of C – H bond in acetylene is nearer to carbon, which has 50% s-character

 

Question: Propyne can be prepared by dehydrohalogenation of

  • a) 1, 2–dichloropropane
  • b) 1, 2–dichloroethane
  • c) 1, 1, 2, 2–tetrachloroethane
  • d) 1–chloropropane

Answer: 1, 2–dichloropropane

 

Question:

  • a) Ammonical silver nitrate.
  • b) Bromine in acetic acid
  • c) Bromine in carbon tetrachloride
  • d) None of these

Answer: Ammonical silver nitrate.

 

Question:

  • a)

  • b)

  • c)

  • d) None of these

Answer:

 

Question:

  • a) 1 < 2 < 3
  • b) 3 < 2 < 1
  • c) 2 < 3 < 1
  • d) 1 < 3 < 2

Answer: 1 < 2 < 3

 

Question:

  • a)

  • b) None of these
  • c)

  • d)

Answer:

 

Question:

  • a) (i) and (iv)
  • b) (i) and (iii)
  • c) (ii) and (iv)
  • d) (i) and (iv)

Answer: (i) and (iv)

 

Question: Which one of these is not compatible with arenes?

  • a) Electrophilic additions
  • b) Resonance
  • c) Greater stability
  • d) None of these

Answer: Electrophilic additions

 

Question:

  • a) Functional isomer
  • b) Position isomer
  • c) Chain isomer
  • d) Stereoisomer

Answer: Functional isomer

 

Question: The carbon-carbon bond length in benzene is

  • a) In between C2H6 and C2H4
  • b) In between C2H4 and C2H2
  • c) Same as in C2H4
  • d) None of these

Answer: In between C2H6 and C2H4

 

Question: Point out the wrong statement in relation to the structure of benzene

  • a) It forms only one monosubstitution product
  • b) The C - C bond distance in benzene is uniformly 1.397Å
  • c) It is a resonance hybrid of a number of canonical forms
  • d) None of these

Answer: It forms only one monosubstitution product

 

Question:

  • a) 4
  • b) 2
  • c) 3
  • d) 8

Answer: 4

 

Question:

  • a) 6 p-orbitals and 6 unpaired electrons
  • b) 6 p-orbitals and 7 unpaired electrons
  • c) 7 p-orbitals and 7 unpaired electrons
  • d) 7 p-orbitals and 6 unpaired electrons

Answer:  6 p-orbitals and 6 unpaired electrons

 

Question: (i) Chlorobenzene and (ii) benzene hexachloride are obtained from benzene by the reaction of chlorine, in the pesence of

  • a) (i) Direct sunlight and (ii) anhydrous AlCl3
  • b) (i) Sodium hydroxide and (ii) sulphuric acid
  • c) (i) Ultraviolet light and (ii) anhydrous FeCl3
  • d) (i) Anhydrous AlCl3 and (ii) direct sunlight

Answer: (i) Direct sunlight and (ii) anhydrous AlCl3

 

Question: A group which deactivates the benzene ring towards electrophilic substitution but which directs the incoming group principally to the o- and p-positions is

  • a) –Cl
  • b) –C2H5
  • c) –NH2
  • d) –NO2

Answer:  –Cl

 

Question: Benzene can be obtained by heating either benzoic acid with X or phenol with Y. X and Y are respectively.

  • a) Soda lime and zinc dust
  • b) Zinc dust and soda lime
  • c) Zinc dust and sodium hydroxide
  • d) Soda lime and copper

Answer: Soda lime and zinc dust

 

Question:  Which of the following chemical system is non aromatic?

  • a)

  • b)

  • c)

  • d) None of these

Answer:

 

Question: Which of the following statements is false for isopentane

  • a) It has a carbon which is not bonded to hydrogen
  • b) It has one CH group
  • c) It has one CH2 group
  • d) None of these

Answer: It has a carbon which is not bonded to hydrogen

 

MCQs for Hydrocarbons Chemistry Full Syllabus

Expert teachers of studiestoday have referred to NCERT book for Full Syllabus Chemistry to develop the Chemistry Full Syllabus MCQs. If you download MCQs with answers for the above chapter you will get higher and better marks in Full Syllabus test and exams in the current year as you will be able to have stronger understanding of all concepts. Daily Multiple Choice Questions practice of Chemistry will help students to have stronger understanding of all concepts and also make them expert on all critical topics. After solving the questions given in the MCQs which have been developed as per latest books also refer to the NCERT solutions for Full Syllabus Chemistry. We have also provided lot of MCQ questions for Full Syllabus Chemistry so that you can solve questions relating to all topics given in each chapter. After solving these you should also refer to Full Syllabus Chemistry MCQ Test for the same chapter.

Where can I download latest JEE (Main) MCQs for Full Syllabus Chemistry Hydrocarbons

You can download the JEE (Main) MCQs for Full Syllabus Chemistry Hydrocarbons for latest session from StudiesToday.com

Are the Full Syllabus Chemistry Hydrocarbons MCQs available for the latest session

Yes, the MCQs issued by JEE (Main) for Full Syllabus Chemistry Hydrocarbons have been made available here for latest academic session

Where can I find JEE (Main) Full Syllabus Chemistry Hydrocarbons MCQs online?

You can find JEE (Main) Full Syllabus Chemistry Hydrocarbons MCQs on educational websites like studiestoday.com, online tutoring platforms, and in sample question papers provided on this website.

How can I prepare for Hydrocarbons Full Syllabus MCQs?

To prepare for Hydrocarbons MCQs, refer to the concepts links provided by our teachers and download sample papers for free.

Are there any online resources for JEE (Main) Full Syllabus Chemistry Hydrocarbons?

Yes, there are many online resources that we have provided on studiestoday.com available such as practice worksheets, question papers, and online tests for learning MCQs for Full Syllabus Chemistry Hydrocarbons