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Hydrocarbons Test - 23

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Hydrocarbons Test - 23
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  • Question 1
    1 / -0
    How many isomers are possible in $$C_4H_8$$?
    Solution

    There are five constitutional isomers with the formula $${ C }_{ 4 }{ H }_{ 8 }$$. They are

    1. But-1-ene
    2. But-2-ene
    3. 2-Methylpropane
    4. Cyclobutane
    5. methylcyclopropane


    Hence, this is the answer.

  • Question 2
    1 / -0
    The IUPAC name of given compound is:

    $$CH_3-C\equiv C-C(CH_3)_2-CH_3$$
    Solution
    $$ CH_3-C\equiv C-C(CH_3)_2-CH_3$$

    IUPAC name: 4,4-dimethyl-pent-2-yne
  • Question 3
    1 / -0
    How many isomers are possible for $$C_6H_{12}$$?
    Solution

    If we limited it to straight-chained alkenes and any conventional cycloalkanes (i.e. the reasonable ones that we would be expected to think of), then there are six. But let's just get as many of the down as we can think of.

  • Question 4
    1 / -0
    Give IUPAC name of the following compound :
    $$CH\equiv C-C(CH_3)_3$$
    Solution
    $$\underset {1}{C}H\equiv \underset{2}{C}- \underset{3}{C}(CH_3)_2-\underset{4}{C}H_3$$

    The numbering of the compound starts from the triple bond carbon, as alkynes are given higher priority in the order of priority of functional groups when compared to alkanes or single bonds, and methyl substituents.

    IUPAC name: 3,3 - dimethylbutyne.

    Hence, the correct option is B.
  • Question 5
    1 / -0
    The degree of unsaturation of the compound formed by the partial hydrogenation of phenol is:
    Solution
    The degree of unsaturation of the compound formed by the partial hydrogenation of phenol is 2.
    Phenol has 3 $$\displaystyle C=C$$ double bonds. During the partial hydrogenation of phenol, one
    $$\displaystyle C=C$$ double is hydrogenated and two $$\displaystyle C=C$$ double bonds remain.

  • Question 6
    1 / -0
    The IUPAC name of the compound $$CH\equiv C-CH_2-CH_2-CH=CH_2$$ is:
    Solution
    $$CH\equiv C-CH_2-CH_2-CH=CH_2$$

    IUPAC name:  Hex-1-en-5-yne.

    Numbering starts from the double bond bearing carbon, as alkenes are higher priority functional groups than alkynes (triple bond).
  • Question 7
    1 / -0
    The correct structural formula of benzene is :
    Solution
    The correct structural formula of benzene is represented by the option (B). Here one H atom is attached to each C atom. In the 6 member ring, alternate single and double bonds are present. Each C atom is sp$$\displaystyle _2$$ hybridised as in ethylene molecule. 3 C$$\displaystyle =$$C double bonds are completely delocalised over entire ring.

  • Question 8
    1 / -0
    IUPAC name of the first member of alkyne is ___________.
    Solution
    Alkynes are carbon compounds with general formula $$C_nH_{2n-2}$$
    The first member of alkyne series is $$C_2H_2$$ (ethyne)
    $$H-C\equiv C-H$$
    Alkyne series: $$C_2H_2, C_3H_4, C_4H_6, C_5H_8$$.
  • Question 9
    1 / -0
    The compound which is not formed when a mixture of n-butyl bromide and ethyl bromide treated with sodium metal in presence of dry ether is :
    Solution
    The compound which is not formed when a mixture of n-butyl bromide and ethyl bromide treated with sodium metal in the presence of dry ether is ethane, $$\displaystyle CH_3-CH_3$$.

    The following products are obtained during the reaction.

    $$\displaystyle  2\underset {\displaystyle  ethyl \: bromide}{ CH_3-CH_2- Br}\xrightarrow [dry \: ether]{Na} \underset {\displaystyle  butane}{CH_3-CH_2-CH_2-CH_3}$$

    $$\displaystyle  2\underset {\displaystyle  n-butyl \: bromide}{ CH_3-CH_2-CH_2-CH_2-Br}\xrightarrow [dry \: ether]{Na} \underset {\displaystyle  octane}{CH_3-CH_2-CH_2-CH_2-CH_2-CH_2-CH_2-CH_3}$$

    $$\displaystyle  \underset {\displaystyle  n-butyl \: bromide}{ CH_3-CH_2-CH_2-CH_2-Br}+ \underset {\displaystyle  ethyl \: bromide}{ CH_3-CH_2- Br}\xrightarrow [dry \: ether]{Na} \underset {\displaystyle  hexane}{CH_3-CH_3}$$

    So, the corret option is $$D$$
  • Question 10
    1 / -0
    Which of the compound does not dissolve in concentrated $$H_2SO_4$$?
    Solution
    $$\displaystyle Hexane$$ does not dissolve in concentrated $$\displaystyle H_2SO_4$$. $$\displaystyle Hexane$$ is nonpolar hydrocarbon. Polar compound such as $$\displaystyle benzene$$, $$\displaystyle ethylene$$ and $$\displaystyle aniline$$ dissolve in concentrated $$\displaystyle H_2SO_4$$ as they donate their $$\displaystyle \pi$$ electrons to $$\displaystyle H^+$$ ions of concentrated $$\displaystyle H_2SO_4$$.

    Option A is correct.
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