Q.Write structural formulas of the following compounds :
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Start your 14-day free trial to unlock the full solution →Draw the longest carbon chain first, number it correctly, then attach the methyl substituents at the positions specified in the IUPAC name. (i) has a 7-carbon chain with four methyls; (ii) has a 6-carbon chain with two methyls.
Understanding Chain Isomerism and IUPAC Nomenclature
When you see a systematic IUPAC name, it's a precise instruction manual for building the molecule. The parent name (heptane, hexane) tells you the length of the longest continuous carbon chain. The numbers and prefixes (3,4,4,5-tetramethyl) tell you exactly where to attach the branches and how many there are.
The key insight: always draw the parent chain first, number the carbons, then add substituents like decorating a Christmas tree.
(i) 3,4,4,5–Tetramethylheptane
Step-by-step construction:
- Identify the parent chain. "Heptane" means a 7-carbon straight chain. Draw it:
- Number the chain. Number from left to right (or right to left—either works, but be consistent):
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Decode the substituents.
"3,4,4,5-Tetramethyl" means four methyl groups () attached at positions 3, 4, 4, and 5. Notice position 4 appears twice—that carbon carries two methyl groups.
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Attach the methyls.
- One on carbon-3
- Two groups on carbon-4
- One on carbon-5
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Complete the structure with hydrogens.
Each carbon forms four bonds total. Fill remaining valences with hydrogen.
Structural formula:
Or in condensed form:
A common mistake is forgetting that carbon-4 has two methyl groups. The locant "4" appears twice in "3,4,4,5," which means carbon-4 is a quaternary carbon (bonded to four other carbons, no hydrogens).
(ii) 2,5-Dimethylhexane
Step-by-step construction:
- Identify the parent chain. …
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