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A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?
- a)5-methyl-1,3-cyclopentadiene
- b)1,4-dimethylcyclobutadiene
- c)1-etheny1-3-methylcyclopropene
- d)3-methyl-1-pentene-4-yne
Correct answer is option 'D'. Can you explain this answer?
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A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic...
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A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic...
Baki sb option mai 6hydrogen k attach hone k liye bond available nhi h
d is the only ans having a triple bond and a double bond and 3rd no. carbon is chiral toooo
6 hydrogen bcz mw of hydrocarbon =80
and after hydrogenation 86
86-80 =6
d is the only ans having a triple bond and a double bond and 3rd no. carbon is chiral toooo
6 hydrogen bcz mw of hydrocarbon =80
and after hydrogenation 86
86-80 =6
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A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic...
Introduction:
The question asks us to identify the hydrocarbon with the molecular formula C6H8 that is chiral but becomes achiral upon catalytic hydrogenation, resulting in a hydrocarbon with a molar mass of 86 g/mol.
Explanation:
To determine the correct answer, let's analyze each option and eliminate the incorrect ones.
Option A: 5-methyl-1,3-cyclopentadiene
- The molecular formula is C6H8, which matches the given information.
- However, this compound does not contain any double bonds, which means it cannot undergo catalytic hydrogenation to become achiral.
- Therefore, option A is incorrect.
Option B: 1,4-dimethylcyclobutadiene
- The molecular formula is C6H8, which matches the given information.
- This compound contains two double bonds, which can undergo catalytic hydrogenation to become achiral.
- However, upon catalytic hydrogenation, the molar mass of this compound would increase, as hydrogen atoms would be added to the double bonds.
- Therefore, option B is incorrect.
Option C: 1-ethenyl-3-methylcyclopropene
- The molecular formula is C6H8, which matches the given information.
- This compound contains one double bond, which can undergo catalytic hydrogenation to become achiral.
- However, upon catalytic hydrogenation, the molar mass of this compound would increase, as hydrogen atoms would be added to the double bond.
- Therefore, option C is incorrect.
Option D: 3-methyl-1-pentene-4-yne
- The molecular formula is C6H8, which matches the given information.
- This compound contains one double bond and one triple bond. Upon catalytic hydrogenation, both the double bond and triple bond would be converted to single bonds, resulting in an achiral compound.
- The molar mass of this compound is 86 g/mol, which matches the given information.
- Therefore, option D is the correct answer.
Conclusion:
Among the given options, the hydrocarbon with the molecular formula C6H8 that is chiral but becomes achiral upon catalytic hydrogenation, resulting in a molar mass of 86 g/mol, is option D: 3-methyl-1-pentene-4-yne.
The question asks us to identify the hydrocarbon with the molecular formula C6H8 that is chiral but becomes achiral upon catalytic hydrogenation, resulting in a hydrocarbon with a molar mass of 86 g/mol.
Explanation:
To determine the correct answer, let's analyze each option and eliminate the incorrect ones.
Option A: 5-methyl-1,3-cyclopentadiene
- The molecular formula is C6H8, which matches the given information.
- However, this compound does not contain any double bonds, which means it cannot undergo catalytic hydrogenation to become achiral.
- Therefore, option A is incorrect.
Option B: 1,4-dimethylcyclobutadiene
- The molecular formula is C6H8, which matches the given information.
- This compound contains two double bonds, which can undergo catalytic hydrogenation to become achiral.
- However, upon catalytic hydrogenation, the molar mass of this compound would increase, as hydrogen atoms would be added to the double bonds.
- Therefore, option B is incorrect.
Option C: 1-ethenyl-3-methylcyclopropene
- The molecular formula is C6H8, which matches the given information.
- This compound contains one double bond, which can undergo catalytic hydrogenation to become achiral.
- However, upon catalytic hydrogenation, the molar mass of this compound would increase, as hydrogen atoms would be added to the double bond.
- Therefore, option C is incorrect.
Option D: 3-methyl-1-pentene-4-yne
- The molecular formula is C6H8, which matches the given information.
- This compound contains one double bond and one triple bond. Upon catalytic hydrogenation, both the double bond and triple bond would be converted to single bonds, resulting in an achiral compound.
- The molar mass of this compound is 86 g/mol, which matches the given information.
- Therefore, option D is the correct answer.
Conclusion:
Among the given options, the hydrocarbon with the molecular formula C6H8 that is chiral but becomes achiral upon catalytic hydrogenation, resulting in a molar mass of 86 g/mol, is option D: 3-methyl-1-pentene-4-yne.
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A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer?
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A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer? for Class 11 2024 is part of Class 11 preparation. The Question and answers have been prepared according to the Class 11 exam syllabus. Information about A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer? covers all topics & solutions for Class 11 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer?.
A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer? for Class 11 2024 is part of Class 11 preparation. The Question and answers have been prepared according to the Class 11 exam syllabus. Information about A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer? covers all topics & solutions for Class 11 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer?.
Solutions for A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer? in English & in Hindi are available as part of our courses for Class 11.
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A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer?, a detailed solution for A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer? has been provided alongside types of A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer? theory, EduRev gives you an
ample number of questions to practice A hydrocarbon with molecular formula C6H8 is chiral but upon catalytic hydrogenation gives achiral hydrocarbon of molar mass 86. Which of the following could be the starting compound?a)5-methyl-1,3-cyclopentadieneb)1,4-dimethylcyclobutadienec)1-etheny1-3-methylcyclopropened)3-methyl-1-pentene-4-yneCorrect answer is option 'D'. Can you explain this answer? tests, examples and also practice Class 11 tests.
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