The Williamson's synthesis reaction among the following is -
1. | |
2. | |
3. | \(C_2H_5I + C_2H_5ONa \rightarrow C_2H_5-O-C_2H_5 + NaI\) |
4. |
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Match the following:
List I | List II | ||
i. | O2N-C6H5-OCH3 (p) | a. | 4-Ethoxy-1,1-dimethylcyclohexane |
ii. | C2H5OCH2-CH(CH3)2 | b. | 1-Chloro-2-methoxyethane |
iii. | CH3OCH2CH2Cl | c. | 1-Ethoxy-2-methylpropane |
iv. | |
d. | 1-Methoxy-4-nitrobenzene |
i | ii | iii | iv | |
1. | d | c | b | a |
2. | c | d | b | a |
3. | a | c | b | d |
4. | b | c | d | a |
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Match the starting material in Column I with the products formed (Column II) in the reaction with HI.
Column I |
Column II |
||
A. | 1. | |
|
B. | |
2. | |
C. | |
3. | |
D. | |
4. | |
5. | |
A | B | C | D | |
1. | 2 | 3 | 4 | 1 |
2. | 3 | 1 | 5 | 2 |
3. | 5 | 4 | 3 | 2 |
4. | 4 | 5 | 2 | 1 |
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Match the items of Column I with items of Column II.
Column l |
Column ll |
||
A. |
Reimer-Tiemann reaction |
1. |
Conversion of phenol to o-hydroxysalicylic aid |
B. |
Kolbe's reaction |
2. |
Heated copper at 573K |
C. |
Conversion of 2alcohol to a ketone |
3. |
Reaction of an alkyl halide |
D. |
Williamson's synthesis |
4. |
Conversion of phenol to salicylaldehyde |
Codes
A | B | C | D | |
1. | 2 | 3 | 4 | 1 |
2. | 3 | 4 | 1 | 2 |
3. | 1 | 4 | 3 | 2 |
4. | 4 | 1 | 2 | 3 |
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Among the following ethers, the one that will produce methyl alcohol on treatment with hot concentrated HI is:
1. | 2. | |
|
3. | |
4. |
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Preparation of ethers by 2 or 3-degree alcohols in an acidic medium is not a suitable method because:
1. | In case of secondary or tertiary alcohols, ketone is obtained as a product. |
2. | In case of secondary or tertiary alcohols, aldehyde is obtained as a product. |
3. | In case of secondary or tertiary alcohols, alkene is obtained as a product. |
4. | In case of primary alcohols, alkene is obtained as a product. |
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The product formed in the below-mentioned reaction is:
1. | |
2. | |
3. | |
4. | |
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CH3 — O — CH(CH3)2 + HI → B (Product)
The product 'B' in the above mentioned reaction is-
1. CH3OH + (CH3)2CHl
2. lCH2OCH(CH3)2
3. CH3OC(CH3)2
4. CH3l + (CH3)2CHOH
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