| Class XII |
Chemistry |
Chemistry-II |
3 |
(i) Cyanohydrin (ii) Acetal (iii) Semicarbazone (iv) Aldol (v) Hemiacetal (vi) Oxime (vii) Ketal (vii) Imine (ix) 2,4-DNP-derivative (x) Schiff’s b... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
nucleophile and which as electrophile. 8.10 An organic compound with the molecular formula C H9O10orms 2,4-DNP derivative, reduces Tollens’ reagent... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
material, reagent or products 8.18 Give plausible explanation for each of the following: (i) Cyclohexanone forms cyanohydrin in good yield but 2,2,... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
Unit Objectives Amines After studying this Unit, you will be able to describe amines as derivatives of “The chief commercial use of amines is as in... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
amines. The fourth orbital of nitrogen in all amines contains an unshared pair of electrons. Due to the presence of unshared pair of electrons, the... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
2roups and suitable prefix such as di, tri, etc. is attached to the amine. The letter ‘e’ of the suffix of the hydrocarbon part is retained. For ex... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
presence of finely divided nickel, palladium or platinum and also by reduction with metals in acidic medium. Nitroalkanes can also be similarly red... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
produce primary amines. This reaction is used for ascent of amine series, i.e., for preparation of amines containing one carbon atom more than the ... |
|
| Class XII |
Chemistry |
Chemistry-II |
4 |
N-dimethylaniline (iii) Cl–(C2 4 –Cl into hexan-1,6-diamine? The lower aliphatic amines are gases with fishy odour. Primary amines 9.5 Physical wit... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
Alkanes of Similar Molecular Masses Sl. No. Compound Molar mass b.p./K 1. n-C 4 9H 2 73 350.8 2. (C2H 5 2H 73 329.3 3. C 2 5(CH )3 2 73 310.5 4. C ... |
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| Class XII |
Computer Science |
Computer Science |
4 |
from where queue was joined) current booth and join Activity 4.3 queue at the vacant booth. In a deque, if insertion and deletion of Following are ... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
3 b R NH 2 pK b –log K b Larger the value of K ob smaller the value of pK , strbnger is the base. The pK values of few amines are given i... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
of the acid. Moreover, the substituted ammonium ion formed from the amine gets stabilised due to dispersal of the positive charge by the +I effect ... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
decides the basic strength of alkyl amines in the aqueous state. The order of basic strength in case of methyl substituted amines and ethyl substit... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
C H NH 2 5 2 2 5 2 3 6 5 2 2. Alkylation Amines undergo alkylation on reaction with alkyl halides (refer Unit 6, Class XII). 3. Acylation Aliphatic... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
with nitrous acid at low temperatures (273-278 K) to form diazonium salts, a very important class of compounds used for synthesis of a variety of a... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
of aromatic amines is that of their very high reactivity. Substitution tends to occur at ortho- and para-positions. If we have to prepare monosubst... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
, C2H N6 , 5H , 2 H CH 3H a6d (5 H )2NH 2 2 5 2 (ii) C H NH , (C H ) NH, (C H ) N, C H NH 2 5 2 2 5 2 2 5 3 6 5 2 (iii) CH NH , (CH ) NH, (CH ) N, ... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
a short time in solution at low temperatures (273-278 K). The stability of arenediazonium ion is explained on the basis of resonance. Benzenediazon... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
halogen acid in the presence of copper powder. This is referred as Gatterman reaction. The yield in Sandmeyer reaction is found to be better than G... |
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| Class XII |
Chemistry |
Chemistry-II |
5 |
-form (m.p. 423 K) is obtained by crystallisation from hot and saturated aqueous solution at 371 K. This behaviour could not be explained by the op... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
be prepared by direct halogenation. Synthesis The cyano group cannot be introduced by nucleophilic substitution of of Aromatic chlorine in chlorobe... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
electrons on nitrogen. Influence of the number of hydrogen atoms at nitrogen atom on the type of reactions and nature of products is responsible fo... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
undergo Friedel-Crafts reaction. (vi) Diazonium salts of aromatic amines are more stable than those of aliphatic amines. (vii) Gabriel phthalimide ... |
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| Class XII |
Chemistry |
Chemistry-II |
4 |
to toluene (ix) Aniline to benzyl alcohol. 9.9 Give the structures of A, B and C in the following reactions: NaCN OH NaOH Br (i) CH 3H I2 A... |
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