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How will you convert Cl−(CH2)4−Cl into hexan-1, 6-diamine? - Chemistry

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प्रश्न

How will you convert Cl−(CH2)4−Cl into hexan-1, 6-diamine?

रासायनिक समीकरण/संरचनाएँ
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उत्तर

\[\ce{Cl-(CH2)4-Cl ->[2 mol NaCN][EtOH] NC-(CH2)4-CN ->[H2/Ni][Reduction] \underset{Hexan-1, 6-diamine}{H2NH2C-(CH2)4-CH2NH2}}\]

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अध्याय 9: Amines - Intext Questions [पृष्ठ २६५]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
अध्याय 9 Amines
Intext Questions | Q 9.3 (iii) | पृष्ठ २६५

संबंधित प्रश्न

Give reasons for the following: (CH3)2NH is more basic than (CH3)3N in an aqueous solution.


Give reason for the following:

Primary amines have higher boiling point than tertiary amines.


Arrange the following: C2H5NH2, C2H5OH, (CH3)3N – in the increasing order of their boiling point


Arrange the following in increasing order of their basic strength :

C6H5 – NH2, C6H5 – CH2 – NH2, C6H5 – NH – CH3


  1. Write structures of different isomeric amines corresponding to the molecular formula C4H11N.
  2. Write the IUPAC names of all the isomers.
  3. What type of isomerism is exhibited by different pairs of amines?

Arrange the following in increasing order of their basic strength:

C2H5NH2, (C2H5)2NH, (C2H5)3N, C6H5NH2


Arrange the following in increasing order of their basic strength:

CH3NH2, (CH3)2NH, (CH3)3N, C6H5NH2, C6H5CH2NH2


Complete the following acid-base reaction and name the product:

\[\ce{CH3CH2CH2NH2 + HCl ->}\]


Account for the following:

Gabriel phthalimide synthesis is preferred for synthesising primary amines.


Arrange the following:

In increasing order of boiling point:

C2H5OH, (CH3)2NH, C2H5NH2


Accomplish the following conversion:

Aniline to p-bromoaniline


Give a plausible explanation for the following:

Why are aliphatic amines stronger bases than aromatic amines?


Give reasons CH3NH2 is more basic than C6H5NH2.


Give reason (CH3)2NH is more basic than (CH3)3N in an aqueous solution.


Tertiary amines have lowest boiling points because ________________


Assertion: N-Ethylbenzene sulphonamide is soluble in alkali.

Reason: Hydrogen attached to nitrogen in sulphonamide is strongly acidic.


The correct order of decreasing basic strength of the given amines is:


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