(a)
Interpretation:
The product for given reaction should be determined.
Concept Introduction:
Acid Catalysed addition of water: When water is added to alkyne in the presence of an acid, the product formed will be an enol. Enol contains a double bond and a
If a carbonyl group is bonded to two alkyl groups, it is called as a
Conversion of terminal
(b)
Interpretation:
The product for given reaction should be determined.
Concept Introduction:
Acid Catalysed addition of water: When water is added to alkyne in the presence of an acid, the product formed will be an enol. Enol contains a double bond and a
If a carbonyl group is bonded to two alkyl groups, it is called as a ketone. The enol formed in the acid catalysed addition of water will be easily converted into a ketone.
Conversion of terminal alkynes into enol: If we want to convert terminal alkyne into an enol, the presence of mercuric ion as a catalyst should be needed and the catalyst will increase the rate of the reaction.
(c)
Interpretation:
The product for given reaction should be determined.
Concept Introduction:
Deprotonation: The reaction in which proton is removed from the compound using reagents is known as deprotonation.
Different reagents are used for the deprotonation and one of the common reagent is sodium amide.
Lindlar catalyst: The catalyst is used for the hydrogenation of alkynes in a syn manner. This means both hydrogen are added on the same side across the triple bond and the product obtained will be a cis product.
Sodium in liquid ammonia: The catalyst is used for the formation of trans alkenes from alkynes. Because of its more reactivity towards triple bonds, the reaction will stop at the formation of alkenes.
(d)
Interpretation:
The product for given reaction should be determined.
Concept Introduction:
Deprotonation: The reaction in which proton is removed from the compound using reagents is known as deprotonation.
Different reagents are used for deprotonation and one of the common reagents is sodium amide.
Lindlar catalyst: The catalyst is used for the hydrogenation of alkynes in a syn manner. This means both hydrogen are added on the same side across the triple bond and the product obtained will be a cis product.
Sodium in liquid ammonia: The catalyst is used for the formation of trans alkenes from alkynes. Because of its more reactivity towards triple bonds, the reaction will stop at the formation of alkenes.

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Chapter 6 Solutions
EBK ESSENTIAL ORGANIC CHEMISTRY
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- Predict the organic products that form in the reaction below, and draw the skeletal ("line") structures of the missing organic products. Please include all steps & drawings & explanations.arrow_forwardWhat are the missing reagents for the spots labeled 1 and 3? Please give a detailed explanation and include the drawings and show how the synthesis proceeds with the reagents.arrow_forwardWhat are the products of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.arrow_forward
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