How many molecules of NO2 are in 0.36 moles?
1 answer:
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Answer:
p-fluoronitrobenzene and sodium phenoxide is more appropriate
Explanation:
An ipso substitution is required to form p-nitrophenyl phenyl ether.
For this ipso substitution, an alkoxide anion needs to attack as a nucleophile at the carbon atom attached to fluorine atom and thereby substitute that F atom.
p-nitrophenoxide is an weak nucleophile as compared to phenoxide due to presence of electron withdrawing resonating effect of nitro group at para position.
p-fluoronitrobenzene is a good choice for nucleophilic attack by alkoxide anion as compared to fluorobenzene due to higher positive charge density at carbon atom directly attached to F atom. Higher positive charge density arises due to presence of electron withdrawing resonating effect og nitro group at para position.
So, p-fluoronitrobenzene and sodium phenoxide is more appropriate
Answer:
Explanation:
The missing image is attached below.
The objective of this question is to draw the major product formed from the diagram attached below.
From the diagram attached, we will see the reaction of a tertiary alkyl halide together with a weak nucleophile (ch3ch2oh) undergoing a nucleophilic substitution (SN₁) mechanism to yield a racemic mixture(i.e., compound that is not optically active but contains an equal amount of dextrorotatory and levorotatory stereoisomers) as a product.
