How the following conversion can be carried out?
Benzene to diphenyl.
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  • 1
    How the following conversion can be carried out?
    Benzene to 4-bromonitrobenzene.
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  • 2
    Arrange the compounds of each set in order of reactivity towards $S_N2$ displacement: $1-$Bromobutane, $1-$Bromo$-2,2-$dimethylpropane, $1-$Bromo$-2-$methylbutane, $1-$Bromo$-3-$methylbutane.
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  • 3
    How will you bring about the following conversion?
    Bromomethane to propanone.
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  • 4
    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-Chloro-2-methylbutane.
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  • 5
    Name the following halides according to $\text{IUPAC}$ system and classify them as alkyl, allyl, benzyl $($primary, secondary, tertiary$),$ vinyl or aryl halides: $\ce{CH_3CH=CHC(Br)(CH_3)_2}.$
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  • 6
    How will you convert aniline to bromobenzene?
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  • 7
    Write the structures of the following organic halogen compound.
    2-Chloro-3-methylpentane.
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  • 8
    Which of the products will be major product in the reaction given below? Explain.
    $\text{CH}_3\text{CH}=\text{CH}_2+\text{HI}\xrightarrow{ \ \ \ \ \ \ \ \ }\text{CH}_3\text{CH}_2\text{CH}_2\text{I}+\text{CH}_3\text{CHICH}_3\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{(A)} \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{(B)}$
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  • 9
    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 $S_N1$ mechanism.
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  • 10
    Predict the major product formed when 2-Bromopentane reacts with alcoholic KOH.
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