A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer?

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A chemist isolated a compound A with molecular formula C₇H₁₃Br. A undergoes very fast S_N1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp³-hybridised carbon atoms. Among those five sp³ carbon atoms, three are methyl groups, one CH₂group and one CH group.
It also contains two sp²-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp² carbons.
The compound contains a total of six aliylic hydrogen atoms.
The carbon atom that holds the Br has one H attached to it.
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When compound A reacts with boiling water, it undergoes a S_N1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C₇H₁₄O. Among the two alcohols, B has the —OH group attached to a sp³ carbon atom that has no H -atoms bonded to it.

If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br₂ to . How many different structures of stereoisomers can be drawn for this tribromide?

a)
2
b)
4
c)
8
d)
None of these

Correct answer is option 'C'. Can you explain this answer?

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A chemist isolated a compound A with molecular formula C7H13Br. A unde...

It has three chiral carbon, hence eight stereoisomers.

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A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is treated with ethanolic solution of KOH in boiling condition, a further new compound E (C7H12) is produced as major product by E2 elimination reaction. Which of the following statement will be consistent with E?

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A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the original compound A is treated with LiAIH4 a new compound D(C7H14) would be produced. How many different structure(s) can be drawn for this D ?

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A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.What can be said about the isomerism shown by the two alcohols B and C ?

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A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the —OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer?

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A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the —OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer? for Class 12 2024 is part of Class 12 preparation. The Question and answers have been prepared according to the Class 12 exam syllabus. Information about A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the —OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer? covers all topics & solutions for Class 12 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the —OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer?.

Solutions for A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the —OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer? in English & in Hindi are available as part of our courses for Class 12. Download more important topics, notes, lectures and mock test series for Class 12 Exam by signing up for free.

Here you can find the meaning of A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the —OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the —OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer?, a detailed solution for A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the —OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer? has been provided alongside types of A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the —OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice A chemist isolated a compound A with molecular formula C7H13Br. A undergoes very fast SN1 reaction. Spectroscopic evidence indicated that compound A has the following structural characteristics : It contains five sp3-hybridised carbon atoms. Among those five sp3 carbon atoms, three are methyl groups, one CH2 group and one CH group.It also contains two sp2-hybridised carbon atoms. Also there is only one hydrogen atom attached to sp2 carbons.The compound contains a total of six aliylic hydrogen atoms.The carbon atom that holds the Br has one H attached to it.Working SpaceWhen compound A reacts with boiling water, it undergoes a SN1 reaction and produces two principal products B and C. Both B and C are alcohols with their molecular formula C7H14O. Among the two alcohols, B has the —OH group attached to a sp3 carbon atom that has no H -atoms bonded to it.Q.If the starting compound A is brominated in gas phase in the presence of a Lewis acid catalyst, a tribromide would result from addition of Br2 to . How many different structures of stereoisomers can be drawn for this tribromide?a)2b)4c)8d)None of theseCorrect answer is option 'C'. Can you explain this answer? tests, examples and also practice Class 12 tests.

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