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Alcohols Phenol...

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  • Question 1
    1 / -0

    On oxymercuration-demercuration, the given compound produces the major product:

  • Question 2
    1 / -0

    Allyl phenyl ether can be prepared by heating:

  • Question 3
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    Which of the following compounds will most readily be dehydrated to give alkene under acidic condition?

  • Question 4
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    The major product of the following reaction is:

  • Question 5
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    Sodium ethoxide has reacted with ethanoyl chloride. The compound that is produced in the above reaction is:

  • Question 6
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    Ortho-nitrophenol is less soluble in water than para and meta-nitrophenols because:

  • Question 7
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    Williamson synthesis of ether is an example of:

  • Question 8
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    Arrange the following compounds in order of decreasing acidity:

  • Question 9
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    Directions For Questions

    $$P$$ and $$Q$$ are isomers of dicarboxylic acid $$\mathrm{C}{}_{4}\mathrm{H}_{4}\mathrm{O}_{4}.\ \mathrm{B}$$oth decolorize $$\mathrm{B}\mathrm{r}_{2}/\mathrm{H}_{2}\mathrm{O}$$. On heating, $$P$$ forms the cyclic anhydride. Upon treatment with dilute alkaline $$\mathrm{K}\mathrm{M}\mathrm{n}\mathrm{O}_{4},\ \mathrm{P}$$ as well as $$\mathrm{Q}$$ could produce one or more than one from $$\mathrm{S},\ \mathrm{T}$$ and $$\mathrm{U}$$.

    ...view full instructions

    Compounds formed from P and Q are, respectively:

  • Question 10
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    Directions For Questions

    A tertiary alcohol $$H$$ upon acid catalyzed dehydration gives a product $$I$$. Ozonolysis of $$I$$ leads to compounds $$J$$ and $$K$$. Compound $$J$$ upon reaction with $$KOH$$ gives benzyl alcohol and a compound $$L$$, whereas $$K$$ on reaction with $$KOH$$ gives only $$M$$.

    ...view full instructions


    The structure of compound $$I$$ is:

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