The structure of Hex-2-en-4-ynoic acid is:
| 1. |  | 
| 2. |  | 
| 3. |  | 
| 4. | None of these | 
The correct IUPAC name of the following compound is:
 
| 1. | 2-Ethylhex-3-en-4-one | 2. | 4-Methylhex-3-en-2-one | 
| 3. | 4-Ethylpent-3-en-2-one | 4. | 3-Methylhex -3-en-4-one | 
Match the common names given in Column I with the IUPAC names given in Column II.
| Column l (Common names) | Column ll (IUPAC names) | 
| A. Cinnamaldehyde | 1. Pentanal | 
| B. Acetophenone | 2. Prop-2-enal | 
| C. Valeraldehyde | 3. 1-Phenylethanone | 
| D. Acrolein | 4. 3-Phenylprop-2-en-al | 
Codes:
| A | B | C | D | |
| 1. | 2 | 3 | 4 | 1 | 
| 2. | 3 | 1 | 4 | 2 | 
| 3. | 1 | 4 | 3 | 2 | 
| 4. | 4 | 3 | 1 | 2 | 
| 1. | PhCH2CH2COOH = 3-Phenylpropanoic acid | 
| 2. | (CH3)2C=CHCOOH = 3-Methylbut-2-enoic acid | 
| 3. |  = 2-Methylcyclopentan-1-oic acid | 
| 4. |  = 2,4,6-Trinitrobenzoic acid | 
| Column I | Column II | ||
| a. | 2-Hydroxycyclopentane carbaldehyde | i. |  | 
| b. | Di-sec-butyl ketone | ii. |  | 
| c. | α-Methoxypropionaldehyde | iii. |  | 
| d. | 4-Fluoroacetophenone | iv. |  | 
| 1. | a-iv; b-i; c-iii; d-ii | 2. | a-ii; b-iv; c-i; d-iii | 
| 3. | a-iii; b-i; c-iv; d-ii | 4. | a-iv; b-iii; c-i; d-ii | 
Select the correct option based on the statements below:
| Assertion (A): | The geometry of formaldehyde molecule is planar. | 
| Reason (R): | Formaldehyde molecule contains sp2 hybridized carbon atom. | 
| 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. |