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.
Identify the suitable reagent for the following conversion: $Ph-C(=O)-OCH_3$ $\longrightarrow$ $Ph-CHO$
Why is chlorobenzene resistant to nucleophilic substitution reactions?
If the system of equations \[ x + 2y - 3z = 2, \quad 2x + \lambda y + 5z = 5, \quad 14x + 3y + \mu z = 33 \] has infinitely many solutions, then \( \lambda + \mu \) is equal to:}
The equilibrium constant for decomposition of $ H_2O $ (g) $ H_2O(g) \rightleftharpoons H_2(g) + \frac{1}{2} O_2(g) \quad (\Delta G^\circ = 92.34 \, \text{kJ mol}^{-1}) $ is $ 8.0 \times 10^{-3} $ at 2300 K and total pressure at equilibrium is 1 bar. Under this condition, the degree of dissociation ($ \alpha $) of water is _____ $\times 10^{-2}$ (nearest integer value). [Assume $ \alpha $ is negligible with respect to 1]