(a)
Interpretation:
The synthetic route for the preparation of given transformation should be determined.
Concept Introduction:
Hydrogenation reaction: The hydrogenation is a reduction reaction which results in an addition of hydrogen. Several organic compounds is hydrogenated, it becomes more saturated.
Linder’s catalyst: The
Soda amide: The
(b)
Interpretation:
The synthetic route for the preparation of given transformation should be determined.
Concept Introduction:
Soda amide: The NaNH2/NH3 is a strong base and excellent nucleophile. Its used deprotonated of weak acids and also for elimination reaction.
Anti- Markovnikov addition: These rules describe the regiochemistry where the substituent is bonded to a less substituted carbon, rather than the more substituted carbon. This placed is quite unusual as carbon cations which are commonly formed during alkene or alkyne reactions tend to favor the more substituted carbon.
(c)
Interpretation:
The synthetic route for the preparation of given transformation should be determined.
Concept Introduction:
Markovnikov addition: The addition reaction of parotic acids to a different alkene or alkyne, the hydrogen atom of
Soda amide: The NaNH2/NH3 is a strong base and excellent nucleophile. Its used deprotonated of weak acids and also for elimination reaction.
(d)
Interpretation:
The synthetic route for the preparation of given transformation should be determined.
Concept Introduction:
Soda amide: The NaNH2/NH3 is a strong base and excellent nucleophile. Its used deprotonated of weak acids and also for elimination reaction.
Metal and ammonia reaction: The alkyne involves sodium (Na)/NH3. This end up reducing to alkyne to give the trans (E) alkene.

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Chapter 9 Solutions
ORGANIC CHEMISTRY 3E WPNGC LL SET 1S
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- Provide the reagents for the following reactions.arrow_forwardIf I have 1-bromopropene, to obtain compound Z, I have to add two compounds A1 and A2. Indicate which compounds are needed. P(C6H5)3arrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. O CH3CH2NH2, TSOH Select to Draw >arrow_forward
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