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Identify the product (P) in the given reaction:

1.    2.  
3.   4.  

Subtopic:  Alcohols: Preparation & Properties |
Level 4: Below 35%
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What is the major product (A) in the following reaction?

1. 2. 
3. 4.
Subtopic:  Alcohols: Preparation & Properties |
Level 3: 35%-60%
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Which of the following compounds is most prone to oxidation?
 

1.
\(\mathrm{CH}_3-\mathrm{CHOH}-\mathrm{CH}_3\)
2.   
3.
\(\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{O}-\mathrm{CH}_2-\mathrm{CH}_3\)
4.   
Subtopic:  Alcohols: Preparation & Properties |
Level 3: 35%-60%
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The best reagent to convert pent-3-en-2-ol into pent-3-en-2-one is:

1. Acidic KMnO4

2. Alkaline K2Cr2O7

3. Chromium anhydride in glacial acetic acid

4. Pyridinium Chlorochromate

Subtopic:  Alcohols: Preparation & Properties |
Level 4: Below 35%
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If the starting material is 1-methyl-1,2-epoxy cyclopentane, of absolute configuration, decide which one compound correctly represent the product of its reaction with sodium methoxide in methanol.
 

1. 2.
3. 4. All of above

Subtopic:  Alcohols: Preparation & Properties |
Level 4: Below 35%
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1-Phenoxypropane is treated with an excess of conc. Hl at 0°C and the mixture of products is treated with thionyl chloride. The products formed are:

1. n-propanol + Chlorobenzene
2. Phenol + n-propyl iodide
3. n-propyl chloride + Chlorobenzene
4. n-propyl chloride + Phenol

Subtopic:  Ethers: Preparation & Properties, Uses |
Level 3: 35%-60%
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The order of reactivity of the following Compounds in electrophilic monochlorination at the most favourable position is

1.  I < II < IV < III

2.  III < IV < I < II

3.  IV < III < II < I

4.  III < II < IV < I

Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
Level 3: 35%-60%
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Select the correct option based on statements below:

Assertion (A): Phenol does not react with NaHCO3 but 2,4,6-trinitrophenol does react with the evolution of CO2
Reason (R): 2,4,6-trinitrophenol is a stronger acid than carbolic acid.
  
1. Both (A) and (R) are True and (R) is the correct explanation of (A).
2. Both (A) and (R) are True but (R) is not the correct explanation of (A).
3. (A) is True but (R) is False.
4. (A) is False but (R) is True.
Subtopic:  Phenols: Preparation & Properties |
Level 3: 35%-60%
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Which of the following compounds is/are aromatic alcohol?

1. (A), (B), (C), (D)     2. (A), (D)  
3. (B), (C)  4. (A) Only
Subtopic:  Alcohols: Preparation & Properties |
Level 3: 35%-60%
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The proposed mechanism for hydration of ethene to yield ethanol is as follows:

The wrong step in the above mechanism is:

1. Step 1 2. Step 2
3. Step 3 4. Both steps 2 and 3
Subtopic:  Mechanism of Dehydration, Methanol & Ethanol |
Level 3: 35%-60%
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