



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 reaction of benzene. the percentage of oxygen is _______ %. (Nearest integer) 
Two p-n junction diodes \(D_1\) and \(D_2\) are connected as shown in the figure. \(A\) and \(B\) are input signals and \(C\) is the output. The given circuit will function as a _______. 
A substance 'X' (1.5 g) dissolved in 150 g of a solvent 'Y' (molar mass = 300 g mol$^{-1}$) led to an elevation of the boiling point by 0.5 K. The relative lowering in the vapour pressure of the solvent 'Y' is $____________ \(\times 10^{-2}\). (nearest integer)
[Given : $K_{b}$ of the solvent = 5.0 K kg mol$^{-1}$]
Assume the solution to be dilute and no association or dissociation of X takes place in solution.