Consider The Following Reaction : The Product 'A' Is - 1.C6H5OH 2 ...
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Consider the following reaction:
The product 'A' is:
1. C6H5OH
2. C6H5COCH3
3. C6H5Cl
4. C6H5CHO
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Save changesSubtopic: Name Reaction | 92%Level 1: 80%+AIPMT - 2012Other Reason
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Select Color:Add Note (Optional):Save changes1234Show me in NCERTShow me in VideoView ExplanationAdd NoteMore ActionsHintsLinksMatch the compounds given in List-I with List-II and select the suitable option from the code given below:
| List-I | List-II |
| (a) Benzaldehyde | (i) Phenolphthalein |
| (b) Phthalic anhydride | (ii) Benzoin condensation |
| (c) Phenyl benzoate | (iii) Oil of wintergreen |
| (d) Methyl salicylate | (iv) Fries rearrangement |
Codes:
| (a) | (b) | (c) | (d) | |
| 1. | (ii) | (i) | (iv) | (iii) |
| 2. | (iv) | (i) | (iii) | (ii) |
| 3. | (iv) | (ii) | (iii) | (i) |
| 4. | (ii) | (iii) | (iv) | (i) |
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Select Color:Add Note (Optional):Save changes1234View ExplanationAdd NoteMore ActionsHintsA yellow precipitate with iodine and alkali is given by:
(i) Methyl acetate
(ii) Acetamide
(iii) 2-Hydroxypropane
(iv) Acetophenone
| 1. | (i) and (ii) | 2. | (ii) and (iii) |
| 3. | (iii) and (iv) | 4. | (iv) and (i) |
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Select Color:Add Note (Optional):Save changes1234Show me in NCERTShow me in VideoView ExplanationAdd NoteMore ActionsPrevious DoubtsHintsLinks
Q140:The compound that does not give an iodoform test is:
1. 3-Pentanone
2. 2-Pentanone
3. Ethanol
4. Ethanal
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Save changesSubtopic: Name Reaction | 77%Level 2: 60%+AIPMT - 1998Other Reason
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Select Color:Add Note (Optional):Save changes1234Show me in NCERTShow me in VideoView ExplanationAdd NoteMore ActionsHintsLinksEthylbenzene is obtained from phenyl methyl ketone by using:
1. Zn–Hg+HCl
2. LiAlH4
3. KMnO4
4. None of the above
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Save changesSubtopic: Name Reaction | 80%Level 1: 80%+AIPMT - 1999Other Reason
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Select Color:Add Note (Optional):Save changes1234Show me in NCERTShow me in VideoView ExplanationAdd NoteMore ActionsPrevious DoubtsHintsLinksAn acid that forms an anhydride (X) on heating and an acid imide (Y) on strong heating with ammonia is:
| 1. | ![]() | 2. | ![]() |
| 3. | ![]() | 4. | ![]() |
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Save changesSubtopic: Carboxylic Acids: Preparation & Properties | 83%Level 1: 80%+NEET - 2020Other Reason
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An organic compound with the molecular formula C9H10O forms a 2,4-DNP derivative, reduces Tollens’ reagent, and undergoes the Cannizzaro reaction. On vigorous oxidation, it gives 1,2-benzenedicarboxylic acid. This organic compound will be:
| 1. | 2-Methyl benzaldehyde | 2. | 2-Hydroxy benzaldehyde |
| 3. | 2-Ethyl benzaldehyde | 4. | 4-Ethyl benzaldehyde |
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Save changesSubtopic: Aldehydes & Ketones: Preparation & Properties | 55%Level 3: 35%-60%Other Reason
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Select Color:Add Note (Optional):Save changes1234Show me in NCERTView ExplanationAdd NoteMore ActionsPrevious DoubtsHintsThe below structure is an example of : 
| 1. | Cyanohydrin | 2. | Hemiacetal |
| 3. | Acetal | 4. | Cyanoalcohol |
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Save changesSubtopic: Isomers & Reaction Mechanism | 71%Level 2: 60%+Other Reason
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Q39:The structure of Hex-2-en-4-ynoic acid is:
| 1. | ![]() |
| 2. | ![]() |
| 3. | ![]() |
| 4. | None of these |
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Save changesSubtopic: Carboxylic Acids: Preparation & Properties | 88%Level 1: 80%+Other Reason
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