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CH3-CH2-CH2-CH3    AlCl3/         CH3-CH-CH3
                                                                       l
                                                                       CH3

Above reaction is an example of:-

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Explanation

The given reaction involves the conversion of butane (CH3-CH2-CH2-CH3) to 2-methylpropane (CH3-CH-CH3) using AlCl3 as a catalyst. This rearrangement of the carbon skeleton is known as isomerization, which is an important process in the petroleum industry.

Which of the following reactants is suitable for preparation of methane and ethane by using one step only?

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Explanation

CH3-Br (methyl bromide) can be used to prepare methane (CH4) and ethane (CH3-CH3) in a single step reaction by treating it with a reducing agent like LiAlH4 or Zn/HCl. The alkyl halide (CH3-Br) is reduced to the corresponding alkane by replacing the halogen with hydrogen.

On catalytic reduction(H2/Pt) how many alkenes will give n-butane?

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Explanation

On catalytic reduction with H2/Pt, there are three alkene isomers that can give n-butane as the product: 1-butene, cis-2-butene, and trans-2-butene. These three alkenes will undergo hydrogenation in the presence of the Pt catalyst and hydrogen gas to form n-butane.

Di-imide (N2H2) is used to reduce double bond of:

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Explanation

(d) Di-imide is used to reduce pi-bond formed between like atom.

 For example -CH=CH-, -N=N-

It cannot be reduced following gps.

          O          N-C||-, -C||-,-N=O,-CN-NC

Trans-cyclohexane-1,2-diol can be obtained by the reaction of cyclohexane with:

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The principal organic product formed in the reaction given below is:-
CH2=CH(CH2)8COOH+HBr→...
                                  peroxide

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Explanation

(c) Anti-Markovnikoff's addition take place.

When 2-butyne is treated with Pd-BaSO4; the product formed will be:

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Explanation

(a) Reductive ozonolysis

CH3-CH=CH2(2) CH3CO2T(1) THF:BD3(A); Product (A) of the above reaction is:

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Explanation

In the given reaction, propene (CH3-CH=CH2) undergoes a deuterium (D) exchange reaction in the presence of deuterated tetrahydrofuran (THF:BD3) and a base. The deuterium atoms replace the hydrogen atoms at the α and β positions, leading to the formation of CH3-CHD-CH2D.

In the reaction given below, the product would be :-
                                          OH
                       H3O+                l
CH3-CH=CH-CH3→CH3-CH2-CH-CH3

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CH3-CH2-CH2-CCH+LiHN2(A)(CH3)2SO4(B)

Give the structural formula of compound (B):

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