What is the correct IUPAC name of the below mentioned compound?
1. | 1−Chloro−4−(1−iodophenyl)−3, 3−dimethylbut−1−ene |
2. | 1−Chloro−1−(4−iodophenyl)−3, 3−dimethylbut−1−ene |
3. | 1−Chloro−2−(3−iodophenyl)−3, 3−dimethylbut−1−en |
4. | 4−Chloro−1−(1−iodophenyl)−1, 1−dimethylbut−3−ene |
The number of structural isomers possible for the compound with the formula C4H9Br, is-
1. 5
2. 6
3. 4
4. 2
The reaction below is an example of:
1. Addition reaction.
2.
3. Elimination reaction.
4.
Match the compounds in Column I with their respective effects in Column II:
Column l (Compounds) |
Column lI (Effect) |
A. Chloramphenicol |
I. Malaria |
B. Thyroxine |
II. Anaesthetic |
C. Chloroquine |
III. Typhoid fever |
D. Chloroform |
IV. Goiter |
V. Blood substituent |
Codes:
Options: | A | B | C | D |
1. | II | III | IV | I |
2. | III | IV | I | II |
3. | V | IV | III | II |
4. | IV | V | III | II |
Match the items in Column I and Column II.
Column l | Column ll |
A. SN1 reaction | 1. Vic-dibromide |
B. Elimination of HX from an alkyl halide | 2. Chlorobromocarbons |
C. Bromination of alkenes | 3. Racemisation |
D. Chemicals in fire extinguisher | 4. Saytzeff rule |
Codes:
A | B | C | D | |
1. | 2 | 3 | 4 | 1 |
2. | 3 | 4 | 1 | 2 |
3. | 1 | 4 | 3 | 2 |
4. | 4 | 1 | 3 | 2 |
Match the structures of compounds given in Column I with the classes of compounds given in Column II.
Column I | Column II | ||
A. | ![]() |
1. | Aryl halide |
B. | ![]() |
2. | Alkyl halide |
C. | ![]() |
3. | Vinyl halide |
D. | ![]() |
4. | Allylic halide |
Codes:
A | B | C | D | |
1. | 2 | 4 | 1 | 3 |
2. | 3 | 4 | 1 | 2 |
3. | 1 | 4 | 3 | 2 |
4. | 4 | 1 | 3 | 2 |
Match the reactions given in Column I with the types of reactions given in Column II and mark the appropriate option.
Column-I | Column-II | ||
A. | ![]() |
(i) | Nucleophilic aromatic substitution reaction |
B. | ![]() |
(ii) | Electrophilic aromatic substitution |
C. | ![]() |
(iii) | Saytzeff elimination |
D | ![]() |
(iv) | Electrophilic addition |
(v) | Nucleophilic substitution reaction |
Codes:
A | B | C | D | |
1. | (ii) | (iv) | (v) | (i) |
2. | (iii) | (i) | (v) | (ii) |
3. | (v) | (iv) | (iii) | (ii) |
4. | (iv) | (v) | (iii) | (ii) |
The correct match of column I (Reactions) with column II (Name of reactions) is:
Column I | Column II | ||
A. | ![]() |
1. | Fittig reaction |
B. | ![]() |
2. | Wurtz-Fittig reaction |
C. | ![]() |
3. | Finkelstein reaction |
D. | ![]() |
4. | Sandmeyer reaction |
Codes:
A | B | C | D | |
1. | 2 | 1 | 4 | 3 |
2. | 3 | 1 | 4 | 2 |
3. | 1 | 4 | 3 | 2 |
4. | 4 | 1 | 3 | 2 |
Select the correct option based on statements below:
Assertion (A): | Phosphorus chlorides (tri and Penta) are preferred over thionyl chloride for the preparation of alkyl chlorides from alcohols. |
Reason (R): | Phosphorus chlorides give pure alkyl halides. |
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. | Both (A) and (R) are False. |
Select the correct option based on statements below:
Assertion (A): | The boiling points of alkyl halides decrease in the order RI> RBr > RCl > RF |
Reason (R): | The boiling points of alkyl chlorides, bromides, and iodides are considerably higher than those of the hydrocarbons of comparable molecular mass. |
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. |