Reaction of ethyl formate with excess of CH3MgI followed by hydrolysis gives

1. n-propyl alcohol                 

2. Ethanol             

3. Isopropyl alcohol             

4. Propanal

 

Subtopic:  Alcohols: Preparation & Properties |
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The product that forms when sodium phenoxide is heated with ethyl iodide is-             

1. Phenetole

2. Ethyl phenyl alcohol

3. Phenol

4. None of the above

Subtopic:  Ethers: Preparation & Properties, Uses |
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Among the following sets of reactants which one produces anisole?                           

1. CH3CHO, RMgX

2. C6H5OH, NaOH, CH3I

3. C6H5OH, neutral FeCl3

4. C6H5-CH3, CH3COCl, AlCl3

Subtopic:  Ethers: Preparation & Properties, Uses |
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n-Propyl alcohol and isopropyl alcohol can be chemically distinguished by which reagent:

1. PCl5

2. Reduction

3. Oxidation with potassium dichromate

4. Ozonolysis

Subtopic:  Alcohols: Preparation & Properties |
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Identify the major products P, Q and R in the following sequence of reactions:

1.
2.
3.
4.
Subtopic:  Phenols: Preparation & Properties |
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NEET - 2018

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How many alcohols with molecular formula C4H10O are chiral in nature?

1. 1

2. 2

3. 3

4. 4

Subtopic:  Alcohols: Preparation & Properties |
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Which of the following species acts as the strongest base?

1. \(^\ominus\text{OH}\)
2. \(^\ominus\text{OR}\)
3. \(^\ominus\text{OC}_6\text H_5\)
4.

Subtopic:  Phenols: Preparation & Properties |
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Which of the following compounds will react with sodium hydroxide solution in water?

1. C6H5OH

2. C6H5CH2OH

3. (CH3)3COH

4. C2H5OH

Subtopic:  Phenols: Preparation & Properties |
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Match the structures of the compounds given in Column I with the name of the compounds given in Column II.

   Column I                                           Column II

                                   (a) quinol

                                   (b) Phenetole

                                   (c) Catechol

                                         (d) o-Cresol

                                          (e) Quinone

                                       (f) Resorcinol

                                                                (g) Anisole

1.  (i) — (d), (ii) — (c), (iii) — (f), (iv) — (a); (v) — (g), (vi) — (b)

2.  (i) — (a), (ii) — (d), (iii) — (b), (iv) — (c); (v) — (f), (vi) — (e)

3. (i) — (b), (ii) — (e), (iii) — (a), (iv) — (d); (v) — (g), (vi) — (c)

4.  (i) — (c), (ii) — (b), (iii) — (d), (iv) — (a); (v) — (g), (vi) — (e)

Subtopic:  Alcohols: Preparation & Properties | Ethers: Preparation & Properties, Uses |
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Match the starting materials given in Column I with the products formed by these (Column II) in the reaction with HI.

 

Column I

 

Column II

(i)

CH3-O-CH3

(a)

(ii)

CH3
       \
         CH-O-CH3
      /
CH3

(b)

           CH3
            |
CH3-C-I+CH3OH
            |
           CH3

(iii)

            CH3
             |
H3C-C-O-CH3
             |
            CH3

(c)

+CH3OH

(iv)

(d)

CH3-OH+CH3-I

 

 

(e)

CH3
       \
         CH-OH+CH3I
      /
CH3

 

 

(f)

CH3
       \
         CH-I+CH3OH
      /
CH3

 

 

(g)

          CH3
            |
CH3-C-OH+CH3I
             |
            CH3

1. (i) — (a), (ii) — (e), (iii) — (c), (iv) — (d)

2. (i) — (d), (ii) — (e), (iii) — (b), (iv) — (a)

3. (i) — (b), (ii) — (e), (iii) — (d), (iv) — (a)

4. (i) — (d), (ii) — (a), (iii) — (b), (iv) — (e)

Subtopic:  Ethers: Preparation & Properties, Uses |
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