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An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet at δ1.6 ppm in the 1H NMR spectrum. The compound A is:
  • a)
  • b)
  • c)
  • d)
Correct answer is option 'A'. Can you explain this answer?
Verified Answer
An organic compound A (C8H16O2) on treatment with an excess of methylm...
The chemical reaction involved in the above transformation can be illustrated as

Hence, the compound A is:
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An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet atδ1.6 ppm in the1H NMR spectrum. The compound A is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer?
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An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet atδ1.6 ppm in the1H NMR spectrum. The compound A is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer? for UGC NET 2025 is part of UGC NET preparation. The Question and answers have been prepared according to the UGC NET exam syllabus. Information about An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet atδ1.6 ppm in the1H NMR spectrum. The compound A is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer? covers all topics & solutions for UGC NET 2025 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet atδ1.6 ppm in the1H NMR spectrum. The compound A is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer?.
Solutions for An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet atδ1.6 ppm in the1H NMR spectrum. The compound A is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer? in English & in Hindi are available as part of our courses for UGC NET. Download more important topics, notes, lectures and mock test series for UGC NET Exam by signing up for free.
Here you can find the meaning of An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet atδ1.6 ppm in the1H NMR spectrum. The compound A is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet atδ1.6 ppm in the1H NMR spectrum. The compound A is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer?, a detailed solution for An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet atδ1.6 ppm in the1H NMR spectrum. The compound A is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer? has been provided alongside types of An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet atδ1.6 ppm in the1H NMR spectrum. The compound A is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice An organic compound A (C8H16O2) on treatment with an excess of methylmagnesium chloride generated two alcohols B and C, whereas the reaction of A with lithium aluminum hydride generated only a single alcohol C. Compound B on treatment with an acid yielded an olefin (C6H12), which exhibited only a singlet atδ1.6 ppm in the1H NMR spectrum. The compound A is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer? tests, examples and also practice UGC NET tests.
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