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प्रश्न
Ethylbenzene is generally prepared by acetylation of benzene followed by reduction and not by direct alkylation. Think of a possible reason.
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उत्तर
In (ii) reaction, it readily undergoes further alkylation to produce polysubs- tituted derivative.
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संबंधित प्रश्न
Write the product in the following reaction
Write the product in the following reaction:
How will you bring about the following conversion?
Benzoyl chloride to benzaldehyde.
Write the structure of the product of the following reaction:
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| Column I (Common names) |
Column II (IUPAC names) |
||
| (i) | Cinnamaldehyde | (a) | Pentanal |
| (ii) | Acetophenone | (b) | Prop-2-enal |
| (iii) | Valeraldehyde | (c) | 4-Methylpent-3-en-2-one |
| (iv) | Acrolein | (d) | 3-Phenylprop-2-enal |
| (v) | Mesityl oxide | (e) | 1-Phenylethanone |
Match the acids given in Column I with their correct IUPAC names given in Column II.
| Column I (Acids) |
Column II (IUPAC names) |
||
| (i) | Phthalic acid | (a) | Hexane-1,6-dioic acid |
| (ii) | Oxalic acid | (b) | Benzene-1,2-dicarboxylic acid |
| (iii) | Succinic acid | (c) | Pentane-1,5-dioic acid |
| (iv) | Adipic acid | (d) | Butane-1,4-dioic acid |
| (v) | Glutaric acid | (e) | Ethane-1,2-dioic acid |
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The strongest base among the following
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