
Concept explainers
(a)
Interpretation:
Synthesis method of the given compound has to be given from the compound which have the same number of carbon atoms.
Concept Introduction:
Addition of water to
Under acidic conditions, alkyne reacts with water to produce an enol which then immediately converts into
The formed enol and ketone are called keto-enol tautomers.
Tautomerization: It is the process of inter conversion of tautomers and therefore the process can also be called as keto-enol tautomerization.
Hydroboration reaction:
It is the reaction in which an internal alkyne is converted into ketone. The reagents used for the hydroboration oxidation reaction is either
(b)
Interpretation:
Synthesis method of the given compound has to be given from the compound which have the same number of carbon atoms.
Concept Introduction:
Addition of water to alkynes in presence of acid:
Under acidic conditions, alkyne reacts with water to produce an enol which then immediately converts into ketone. For terminal alkynes, there is a need of catalyst which is mercury.
The formed enol and ketone are called keto-enol tautomers.
Tautomerization: It is the process of inter conversion of tautomers and therefore the process can also be called as keto-enol tautomerization.
Hydroboration reaction:
It is the reaction in which an internal alkyne is converted into ketone. The reagents used for the hydroboration oxidation reaction is either
(c)
Interpretation:
Synthesis method of the given compound has to be given from the compound which have the same number of carbon atoms.
Concept Introduction:
Addition of water to alkynes in presence of acid:
Under acidic conditions, alkyne reacts with water to produce an enol which then immediately converts into ketone. For terminal alkynes, there is a need of catalyst which is mercury.
The formed enol and ketone are called keto-enol tautomers.
Tautomerization: It is the process of inter conversion of tautomers and therefore the process can also be called as keto-enol tautomerization.
Hydroboration reaction:
It is the reaction in which an internal alkyne is converted into ketone. The reagents used for the hydroboration oxidation reaction is either

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Chapter 7 Solutions
Organic Chemistry
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- Organic Functional Groups entifying positions labeled with Greek letters in acids and derivatives 1/5 ssible, replace an H atom on the a carbon of the molecule in the drawing area with a ce an H atom on the ẞ carbon with a hydroxyl group substituent. ne of the substituents can't be added for any reason, just don't add it. If neither substi er the drawing area. O H OH Oneither substituent can be added. Check D 1 Accessibility ado na witharrow_forwardDifferentiate between electrophilic and nucleophilic groups. Give examples.arrow_forwardAn aldehyde/ketone plus an alcohol gives a hemiacetal, and an excess of alcohol gives an acetal. The reaction is an equilibrium; in aldehydes, it's shifted to the right and in ketones, to the left. Explain.arrow_forward
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