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An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can be
- a)CH3OH
- b)CH3COCH3
- c)CH3CHO
- d)CH3CHOHCH3
Correct answer is option 'D'. Can you explain this answer?
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An organic compound X on treatment with acidified k2Cr2O7 gives compou...
D) CH3CHOHCH3 + K2Cr2O7 gives Acetone which gives CHI3 on Haloform Reaction.
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An organic compound X on treatment with acidified k2Cr2O7 gives compou...
Explanation:
Given:
- Organic compound X on treatment with acidified K2Cr2O7 gives compound Y.
- Compound Y reacts with I2 and sodium carbonate to form triiodomethane.
To find:
The compound X.
Solution:
The given reaction can be represented as follows:
X + acidified K2Cr2O7 → Y + other products
Step 1: Oxidation of X:
The acidified K2Cr2O7 acts as an oxidizing agent. It oxidizes the compound X to form compound Y. This indicates that the compound X must have a reducing functional group.
Step 2: Reaction of Y with I2 and sodium carbonate:
Compound Y reacts with I2 and sodium carbonate to form triiodomethane (CHI3). This indicates that compound Y must contain a methyl group (CH3) which can react with I2 to form triiodomethane.
Conclusion:
Based on the given information, we can conclude that the compound X must have a reducing functional group and a methyl group (CH3).
Options:
a) CH3OH (Methanol): It does not have a reducing functional group.
b) CH3COCH3 (Acetone): It does not have a reducing functional group.
c) CH3CHO (Acetaldehyde): It does not have a reducing functional group.
d) CH3CHOHCH3 (2-Propanol): It has a reducing functional group (alcohol) and a methyl group (CH3). This matches the given conditions.
Therefore, the correct answer is option 'D' (CH3CHOHCH3).
Given:
- Organic compound X on treatment with acidified K2Cr2O7 gives compound Y.
- Compound Y reacts with I2 and sodium carbonate to form triiodomethane.
To find:
The compound X.
Solution:
The given reaction can be represented as follows:
X + acidified K2Cr2O7 → Y + other products
Step 1: Oxidation of X:
The acidified K2Cr2O7 acts as an oxidizing agent. It oxidizes the compound X to form compound Y. This indicates that the compound X must have a reducing functional group.
Step 2: Reaction of Y with I2 and sodium carbonate:
Compound Y reacts with I2 and sodium carbonate to form triiodomethane (CHI3). This indicates that compound Y must contain a methyl group (CH3) which can react with I2 to form triiodomethane.
Conclusion:
Based on the given information, we can conclude that the compound X must have a reducing functional group and a methyl group (CH3).
Options:
a) CH3OH (Methanol): It does not have a reducing functional group.
b) CH3COCH3 (Acetone): It does not have a reducing functional group.
c) CH3CHO (Acetaldehyde): It does not have a reducing functional group.
d) CH3CHOHCH3 (2-Propanol): It has a reducing functional group (alcohol) and a methyl group (CH3). This matches the given conditions.
Therefore, the correct answer is option 'D' (CH3CHOHCH3).
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An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer?
Question Description
An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer? for NEET 2024 is part of NEET preparation. The Question and answers have been prepared according to the NEET exam syllabus. Information about An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer? covers all topics & solutions for NEET 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer?.
An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer? for NEET 2024 is part of NEET preparation. The Question and answers have been prepared according to the NEET exam syllabus. Information about An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer? covers all topics & solutions for NEET 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer?.
Solutions for An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer? in English & in Hindi are available as part of our courses for NEET.
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An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer?, a detailed solution for An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer? has been provided alongside types of An organic compound X on treatment with acidified k2Cr2O7 gives compound Y which reacts with I2 and sodium carbonate to form triiodomethane. The compound X can bea)CH3OHb)CH3COCH3c)CH3CHOd)CH3CHOHCH3Correct answer is option 'D'. Can you explain this answer? theory, EduRev gives you an
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