| Class XII |
Chemistry |
Chemistry-II |
2 |
no ether is formed. For example, the reaction of CH ONa with (CH ) C–Br gives exclusively 2-methylpropene. 3 3 3 It is because alkoxides are not on... |
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| Class XII |
Chemistry |
Chemistry-II |
2 |
bonds with water molecule as shown: 7.6.3 Chemical 1. Cleavage of C–O bond in ethers Reactions Ethers are the least reactive of the functional grou... |
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| Class XII |
Chemistry |
Chemistry-II |
2 |
in step 2 of the reaction, the departure of leaving group + (HO–CH )3reatesamorestablecarbocation[(CH ) C ],a3 3hereaction follows SN1 mechanism. I... |
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| Class XII |
Chemistry |
Chemistry-II |
2 |
yield a mixture of ortho and para nitroanisole. Intext Questions 7.10 Write the reactions of Williamson synthesis of 2-ethoxy-3-methylpentane start... |
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| Class XII |
Chemistry |
Chemistry-II |
2 |
to oxidation. The presence of –OH group in phenols activates the aromatic ring towards electrophilic substitution and directs the incoming group to... |
|
| Class XII |
Chemistry |
Chemistry-II |
2 |
7.8 While separating a mixture of ortho and para nitrophenols by steam distillation, name the isomer which will be steam volatile. Give reason. 7.9... |
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| Class XII |
Chemistry |
Chemistry-II |
2 |
propene. (vi) Butan-2-one to butan-2-ol. 7.22 Give reason for the higher boiling point of ethanol in comparison to methoxymethane. 223 Alcohols, Ph... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
Unit Objectives Aldehydes, Ketones After studying this Unit, you will be able to and Carboxylic • write the common and IUPAC names of aldehydes, ke... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
They are used in many food products and pharmaceuticals to add flavours. Some of these families are manufactured for use as solvents (i.e., acetone... |
|
| Class XII |
Chemistry |
Chemistry-II |
3 |
from the carbon of the aldehyde group while in case of ketones the numbering begins from the end nearer to the carbonyl group. The substituents are... |
|
| Class XII |
Chemistry |
Chemistry-II |
3 |
it lie in the same plane and the -electron cloud is above and below this plane. The bond angles are approximately 120° as expected of a trigonal co... |
|
| Class XII |
Chemistry |
Chemistry-II |
3 |
give ketones in this reaction (Unit 9, Class XI). 8.2.2 Preparation 1. From acyl chloride (acid chloride) of Acyl chloride (acid chloride) is hydro... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
reaction is known as Gatterman-Koch reaction. 8.2.3 Preparation 1. From acyl chlorides of Ketones Treatment of acyl chlorides with dialkylcadmium, ... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
alcohols of similar molecular masses due to absence of intermolecular hydrogen bonding. The following compounds of molecular masses 58 and 60 are r... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
the following compounds in increasing order of their boiling points. CH 3HO, CH CH3OH,2CH OCH 3 CH C3 CH 3 2 3 8.4 Chemical Since aldehydes and ket... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
important examples of nucleophilic addition and nucleophilic addition-elimination reactions: (a) Addition of hydrogen cyanide (HCN): Aldehydes and ... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
acid. The equilibrium favours the product formation due to rapid dehydration of the intermediate to form >C=N-Z. Z = Alkyl, aryl, OH, NH , C H NH, ... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
is called cross aldol condensation. If both of them contain -hydrogen atoms, it gives a mixture of four products. This is illustrated below by aldo... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
hence its name carboxyl. Carboxylic acids may be aliphatic (RCOOH) or aromatic (ArCOOH) depending on the group, alkyl or aryl, attached to carboxyl... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
Isobutyric acid 2-Methylpropanoic acid HOOC-COOH Oxalic acid Ethanedioic acid HOOC -CH -C2OH Malonic acid Propanedioic acid HOOC -(CH ) 2 2OH Succi... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
with these oxidising reagents. 3. From nitriles and amides Nitriles are hydrolysed to amides and then to acids in the presence of H or OH as cata... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
masses. This is due to more extensive association of carboxylic acid molecules through intermolecular hydrogen bonding. The hydrogen bonds are not ... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
acids: The esterification of carboxylic acids with alcohols is a kind of nucleophilic acyl substitution. Protonation of the carbonyl oxygen activat... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
known as Hell-Volhard-Zelinsky reaction. 253 Aldehydes, Ketones and Carboxylic Acids Reprint 2026-27 2. Ring substitution Aromatic carboxylic acids... |
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| Class XII |
Chemistry |
Chemistry-II |
3 |
of acyl chloride with dialkylcadmium. A good method for the preparation of aromatic ketones is the Friedel-Crafts acylation of aromatic hydrocarbon... |
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