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Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :
[AIEEE 2011]
- a)1 - Pentene
- b)2 - Pentene
- c)2 - Methyl - 2 - pentene
- d)2 - Methyl - 1 – pentene
Correct answer is option 'C'. Can you explain this answer?
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Ozonolysis of an organic compound ‘A’ produces acetone and...
Solution
Ozonolysis breaks the double bond and oxidizes that carbon. To solve these questions, when the reactants are asked, just remove the carbonyl oxygen from the products and join the resulting compounds using a double bond.
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Ozonolysis of an organic compound ‘A’ produces acetone and...
Ozonolysis is a chemical reaction that involves the cleavage of carbon-carbon double or triple bonds using ozone (O3) as the oxidizing agent. This reaction is commonly used in organic chemistry to determine the structure of unsaturated compounds.
During ozonolysis, the double or triple bond in the organic compound reacts with ozone to form an unstable primary ozonide intermediate. This primary ozonide then undergoes a rearrangement, known as Criegee rearrangement, to form a more stable secondary ozonide. Finally, the secondary ozonide decomposes to yield a variety of products, including aldehydes, ketones, and carboxylic acids.
The products obtained from ozonolysis can provide valuable information about the structure of the original compound. For example, the number of aldehyde or ketone groups formed can indicate the number of carbon-carbon double or triple bonds in the original compound. Additionally, the identity of the specific products can help identify functional groups present in the compound.
Overall, ozonolysis is a useful tool in organic chemistry for determining the structure of unsaturated compounds and studying their reactivity.
During ozonolysis, the double or triple bond in the organic compound reacts with ozone to form an unstable primary ozonide intermediate. This primary ozonide then undergoes a rearrangement, known as Criegee rearrangement, to form a more stable secondary ozonide. Finally, the secondary ozonide decomposes to yield a variety of products, including aldehydes, ketones, and carboxylic acids.
The products obtained from ozonolysis can provide valuable information about the structure of the original compound. For example, the number of aldehyde or ketone groups formed can indicate the number of carbon-carbon double or triple bonds in the original compound. Additionally, the identity of the specific products can help identify functional groups present in the compound.
Overall, ozonolysis is a useful tool in organic chemistry for determining the structure of unsaturated compounds and studying their reactivity.
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Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :[AIEEE 2011]a)1 - Penteneb)2 - Pentenec)2 - Methyl - 2 - pentened)2 - Methyl - 1 – penteneCorrect answer is option 'C'. Can you explain this answer?
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Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :[AIEEE 2011]a)1 - Penteneb)2 - Pentenec)2 - Methyl - 2 - pentened)2 - Methyl - 1 – penteneCorrect answer is option 'C'. 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 Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :[AIEEE 2011]a)1 - Penteneb)2 - Pentenec)2 - Methyl - 2 - pentened)2 - Methyl - 1 – penteneCorrect answer is option 'C'. 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 Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :[AIEEE 2011]a)1 - Penteneb)2 - Pentenec)2 - Methyl - 2 - pentened)2 - Methyl - 1 – penteneCorrect answer is option 'C'. Can you explain this answer?.
Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :[AIEEE 2011]a)1 - Penteneb)2 - Pentenec)2 - Methyl - 2 - pentened)2 - Methyl - 1 – penteneCorrect answer is option 'C'. 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 Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :[AIEEE 2011]a)1 - Penteneb)2 - Pentenec)2 - Methyl - 2 - pentened)2 - Methyl - 1 – penteneCorrect answer is option 'C'. 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 Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :[AIEEE 2011]a)1 - Penteneb)2 - Pentenec)2 - Methyl - 2 - pentened)2 - Methyl - 1 – penteneCorrect answer is option 'C'. Can you explain this answer?.
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Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :[AIEEE 2011]a)1 - Penteneb)2 - Pentenec)2 - Methyl - 2 - pentened)2 - Methyl - 1 – penteneCorrect answer is option 'C'. Can you explain this answer?, a detailed solution for Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :[AIEEE 2011]a)1 - Penteneb)2 - Pentenec)2 - Methyl - 2 - pentened)2 - Methyl - 1 – penteneCorrect answer is option 'C'. Can you explain this answer? has been provided alongside types of Ozonolysis of an organic compound ‘A’ produces acetone and propionaldehyde in equimolar mixture. Identify ‘A’ from the following compounds :[AIEEE 2011]a)1 - Penteneb)2 - Pentenec)2 - Methyl - 2 - pentened)2 - Methyl - 1 – penteneCorrect answer is option 'C'. Can you explain this answer? theory, EduRev gives you an
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