Predict the major product formed when 2-Bromopentane reacts with alcoholic KOH.
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Pent-2-ene is major product known as Saytzeff's Product and it is more stable alkene.
The process is known as $\beta-$ elimination as it involves elimination of $\beta-$ Hydrogen.
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Write the structure of the major organic product in each of the following reaction:
$(\text{CH}_3)_3\text{CBr}+\text{KOH}\xrightarrow[\text{heat}]{\text{ethanol}}$
Predict all the alkenes that would be formed by dehydrohalogenation of the following halides with sodium ethoxide in ethanol and identify the major alkene:
2,2,3-Trimethyl-3-bromopentane.
Read the given passage and answer the questions number $1$ to $5$ that follow$:$
The substitution reaction of alkyl halide mainly occurs by $S_N1$ or $S_N2$ mechanism. Whatever mechanism alkyl halides follow for the substitution reaction to occur, the polarity of the carbon halogen bond is responsible for these substitution reactions. The rate of $S_N1$ reactions are governed by the stability of carbocation whereas for $S_N2$ reactions steric factor is the deciding factor. If the starting material is a chiral compound, we may end up with an inverted product or racemic mixture depending upon the type of mechanism followed by alkyl halide. Cleavage of ethers with $HI$ is also governed by steric factor and stability of carbocation, which indicates that in organic chemistry, these two major factors help us in deciding the kind of product formed.
Predict the stereochemistry of the product formed if an optically active alkyl halide undergoes substitution reaction by $S_N2$ mechanism.