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    4.6 Exercise 1 - Aromatic Chemistry

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    riditha
    The document describes exercises in aromatic chemistry, including describing the shape and bonding of benzene, explaining why benzene does not readily undergo addition reactions, deducing organic products of reactions involving benzene, nitric acid, chloromethane, propene, and propanoyl chloride, providing mechanisms for these reactions, explaining why phenylamine is a weaker base than ethylamine, and listing uses for nitration of benzene, preparation of phenylamine, and preparation of ethylbenzene techniques.

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    4.6 Exercise 1 - Aromatic Chemistry

    Uploaded by

    riditha
    203 views1 page
    The document describes exercises in aromatic chemistry, including describing the shape and bonding of benzene, explaining why benzene does not readily undergo addition reactions, deducing organic products of reactions involving benzene, nitric acid, chloromethane, propene, and propanoyl chloride, providing mechanisms for these reactions, explaining why phenylamine is a weaker base than ethylamine, and listing uses for nitration of benzene, preparation of phenylamine, and preparation of ethylbenzene techniques.

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    The document describes exercises in aromatic chemistry, including describing the shape and bonding of benzene, explaining why benzene does not readily undergo addition reactions, deducing organic products of reactions involving benzene, nitric acid, chloromethane, propene, and propanoyl chloride, providing mechanisms for these reactions, explaining why phenylamine is a weaker base than ethylamine, and listing uses for nitration of benzene, preparation of phenylamine, and preparation of ethylbenzene techniques.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as DOC, PDF, TXT or read online from Scribd
    Download as doc, pdf, or txt
    203 views1 page

    4.6 Exercise 1 - Aromatic Chemistry

    Uploaded by

    riditha
    The document describes exercises in aromatic chemistry, including describing the shape and bonding of benzene, explaining why benzene does not readily undergo addition reactions, deducing organic products of reactions involving benzene, nitric acid, chloromethane, propene, and propanoyl chloride, providing mechanisms for these reactions, explaining why phenylamine is a weaker base than ethylamine, and listing uses for nitration of benzene, preparation of phenylamine, and preparation of ethylbenzene techniques.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as DOC, PDF, TXT or read online from Scribd
    Download as doc, pdf, or txt
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    4.6 EXERCISE 1 AROMATIC CHEMISTRY 1. 2.

    . a) b) Describe the shape of, and bonding in, a molecule of benzene Explain why benzene does not readily undergo addition reactions

    Deduce the main organic products of the following reactions: a) b) c) d) e) benzene with nitric acid in the presence of sulphuric acid benzene with chloromethane in the presence of aluminium chloride benzene with propene in the presence of aluminium chloride and hydrogen chloride benzene with propanoyl chloride in the presence of aluminium chloride nitrobenzene with tin and concentrated hydrochloric acid

    . $. &.

    !i"e mechanisms for the reactions in #a), #b), #c) and #d) Explain why phenylamine is a wea%er base than ethylamine !i"e a use for the following techni'ues in aromatic chemistry: a) b) c) nitration of benzene preparation of phenylamine preparation of ethylbenzene

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