



Naming the Structure: The name “4-Methylpent-2-enal” provides the key structural features of the molecule. The “pent” indicates a five-carbon chain. “2-enal” indicates the presence of a double bond at the second carbon and an aldehyde group at the terminal position. The “4-methyl” substituent specifies a methyl group attached to the fourth carbon.
Construct the Structure Step-by-Step:
Step 1: Place a five-carbon chain.
Step 2: Insert a double bond between carbons 2 and 3.
Step 3: Attach an aldehyde group (C=O with an H) to the first carbon.
Step 4: Add a methyl group to the fourth carbon.
Verify Each Option: Only Option (4) matches this structure, with the correct placement of the double bond, aldehyde group, and methyl substituent.
Conclusion: The structure in Option (4) is correct for 4-Methylpent-2-enal.
To determine the structure of 4-Methylpent-2-enal, we need to first understand the naming and formation of this compound:
Based on this construction, the correct option is identified as follows:
This option accurately reflects the arrangement of carbon atoms and functional groups as described, signifying the correct structure of 4-Methylpent-2-enal. It's essential to follow the IUPAC naming conventions closely to ensure the structure matches the given name.
Consider the following two reactions A and B: 
The numerical value of [molar mass of $x$ + molar mass of $y$] is ___.
Which one of the following graphs accurately represents the plot of partial pressure of CS₂ vs its mole fraction in a mixture of acetone and CS₂ at constant temperature?

Consider the following reaction sequence: 
Given: Compound (x) has percentage composition \(76.6%\ \text{C}\), \(6.38%\ \text{H}\) and vapour density \(=47\). Compound (y) develops a characteristic colour with neutral \(\mathrm{FeCl_3}\) solution. Identify the {INCORRECT statement.}
