Organic Chemistry
Which of the following compounds undergoes nucleophilic substitution reaction most easily?
Rate of the reaction is fastest when $$Z$$ is:
$$Cl^-$$ is the best leaving group being the weakest nucleophile out of $$NH^-_2, Cl^-, OC_2H_5$$ and $$CH_3COO^-$$.
So, when $$Z$$ is $$Cl^-$$, the ion leaves faster thus making the reaction the fastest when $$Z$$ is $$Cl^-$$.
Which of the following compounds undergoes nucleophilic substitution reaction most easily?
$$S_{N}2$$ reaction readily occurs in:
Classify the following reaction in one of the reaction type. $$CH_3CH_2Br+HS^{-}\rightarrow CH_3CH_2SH+Br^{-}$$
The reaction $$CH_3CH_2I+KOH(aq)\rightarrow CH_3CH_2OH +KI$$, is classified as :
The reaction: $$CH_3CH_2I+KOH(aq)\rightarrow CH_3CH_2OH +KI$$ is a nucleophilic substitution. Explain.
The reaction: $$CH_3CH_2I+KOH(aq)\rightarrow CH_3CH_2OH +KI$$ is classified as :
The reaction: $$CH_{3}CH_{2}I + KOH_{(aq.)} \rightarrow CH_{3}CH_{2}OH + KI$$ is classified as:
Identify (B),(C), and (D).
Compound $$(B)$$ is:
How will you bring about the following conversions in not more than two steps? Benzyl alcohol to phenyl ethanenitrile