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प्रश्न
How is nitromethane prepared from the following?
α-nitroalkene
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उत्तर
Preparation of nitromethane from α-nitroalkene:
Nitromethane is prepared by hydrolysis of 2-methyl-1-nitropropene in acidic medium.

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संबंधित प्रश्न
Write the structure of the following compound:
2-Chloro-3-methylpentane
Write the structure of the following compound:
1-Chloro-4-ethylcyclohexane
Write the structure of the following compound:
4-tert. Butyl-3-iodoheptane
Write the structure of the following compound:
1-Bromo-4-sec. butyl-2-methylbenzene
Write structures of different dihalogen derivatives of propane.
Give the IUPAC name of the following compound:
CHF2CBrClF
Give the IUPAC name of the following compound:
CH3C(p-ClC6H4)2CH(Br)CH3
How are the following conversions carried out?
2-methylbutan-1-ol into 2 -methylbutanoic acid.
But-1-ene on reaction with HCl in the presence of sodium peroxide yields _______.
IUPAC name of is C6H5 − CH2 − C − CH2 − CH2 − CH2 − CH3 is _______
(A) 1-Phenylhexan-2-one
(B) 6-Phenylhexan-5-one
(C) 1-Benzylhexan-5-one
(D) Dodecan-5-one
Out of
which is an example of a benzylic halide?
Write the mechanism (using curved arrow notation) of the following reaction:

Write the product(s) in the following reactions:

Write the product(s) in the following reaction:

Write the product(s) in the following reactions:

The compound which contains all the four 1°, 2°, 3° and 4° carbon atoms is:
IUPAC name of (CH3)3CCl:
IUPAC name of CH3CH2C(Br) = CH–Cl is ____________.
Which of the following will have a mesoisomer also?
\[\ce{CH3CH2CH2Cl ->[alc. KOH] B ->[HBr] C ->[Na/ether] D}\]
In the above reaction, the product D is:
In the following sequence of reactions:
\[\ce{C2H5Br ->[AgCN] X ->[Reduction] Y}\]; Y is
Identify Z in the series:
\[\ce{CH2 = CH2 ->[HBr] X ->[aq. KOH] Y ->[Na2CO3][I2 excess] Z}\]
\[\begin{array}{cc}
\ce{CH3-CH-CH=CH2 + HBr -> A}\\
|\phantom{.....................}\\
\ce{CH3}\phantom{..................}
\end{array}\]
'A' is:
Arrange the following compounds in order of decreasing acidity:
| (I) | ![]() |
| (II) | ![]() |
| (III) | ![]() |
| (IV) | ![]() |
Write the structure of the following organic halogen compound.
4-tert-Butyl-3-iodoheptane
Give the IUPAC name of the following compound:
ClCH2C ≡ CCH2Br
Write the structures of the following organic halogen compounds.
1,4-Dibromobut-2-ene
Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3CH2C(CH3)2CH2I
Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
CH3C(C2H5)2CH2Br
Give the IUPAC names of the following compound:
(CCl3)3CCl
Give the IUPAC name of the following compound:
CICH2C ≡ CCH2Br
Write the structure of the following organic halogen compound.
4-tert-Butyl-3-iodoheptane
Give the IUPAC name of the following compound:
\[\ce{(CCl3)3CCl}\]
Give the IUPAC name of the following compound:
\[\ce{(CCl3)3CCl}\]
Give the IUPAC names of the following compound:
\[\ce{ClCH2C ≡ CCH2Br}\]
Write the structure of the following compound:
4-tert-Butyl-3-iodoheptane
Write structure of the following compound:
4-tert. Butyl-3-iodoheptane
Write the structure of the organic halogen compound.
1,4-Dibromobut-2-ene
Write the structure of the following compound:
1,4-Dibromobut-2-ene
Write the structure of the following organic halogen compound.
1,4-Dibromobut-2-ene
Write structure of the following compound:
4-tert. Butyl-3-iodoheptane
Write the structure of the following organic halogen compound.
4 – tert – Butyl -3 -iodoheptane
Write structure of the following compound:
1,4-Dibromobut-2-ene
Name the following halide according to the IUPAC system and classify it as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(Cl)(C2H5)CH2CH3}\]
Name the following halide according to the IUPAC system and classify it as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3CH2C(CH3)2CH2I}\]




