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Q.83 Chemistry ⭐ 360° Option Elimination Active
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NEET 2026 Chemistry Question 83 Solution

Topic: Organic Chemistry: Some Basic Principles and Techniques · Official NTA Booklet Code 50
NEET 2026 Chemistry Question 83: Classification of Polyenes (Conjugated vs Isolated Dienes)

Question

Among the following, the compound having conjugated double bonds is

✓
Verified Against NTA Final Answer Key
Option (1) : hepta-1,3-diene
📚 Organic Chemistry: Some Basic Principles and Techniques Easy
📋 Given Parameters & Problem Setup
Requirement The compound having conjugated double bonds
Options hepta-1,3-diene, hepta-1,4-diene, hepta-1,5-diene, hepta-1,6-diene
⚡

The 30-Second Exam Hall Shortcut: ⚡ Conjugated Double Bond Rule (1,3-relationship)

⏱️ Save ~40 seconds

Alternate double and single bonds (-C=C-C=C-) mean locants differ by 2 (1,3-diene)!

1 Conjugated dienes require two double bonds separated by exactly ONE single bond.
2 In hepta-1,3-diene: C₁=C₂ - C₃=C₄ - C₅ - C₆ - C₇. Double bonds at positions 1 and 3 are separated by a single C₂-C₃ bond -> CONJUGATED!
3 In 1,4-diene: separated by two single bonds (isolated).
4 In 1,5-diene and 1,6-diene: separated by three and four single bonds (isolated).
5 Option (1) is instantly deduced in 5 seconds flat!
🛡️
Why You Can 100% Trust This Shortcut: IUPAC and fundamental organic chemistry definition: A conjugated system has overlapping p-orbitals across alternating single and double bonds.
📐

Step-by-Step Rigorous Workflow & Mathematical Proof

Step 1

Define Conjugated, Isolated, and Cumulated Dienes

1. Conjugated Dienes: Double bonds are separated by exactly one single bond (-C=C-C=C-). Continuous unhybridized p-orbitals allow π-electron delocalization. 2. Isolated Dienes: Double bonds are separated by two or more sp³ hybridized carbon atoms / single bonds (-C=C-(CH₂)ₙ-C=C-). 3. Cumulated Dienes (Allenes): Double bonds are adjacent to the same carbon atom (-C=C=C-).

Conjugated system≡−C=C−C=C−\text{Conjugated system} \equiv -\text{C}=\text{C}-\text{C}=\text{C}-
  • • Delocalization stabilizes the system.
Step 2

Draw and Analyze the Structure of hepta-1,3-diene

Writing the IUPAC structure of hepta-1,3-diene: CH₂=CH-CH=CH-CH₂-CH₂-CH₃

C1=C2−C3=C4−C5−C6−C7\text{C}_1=\text{C}_2-\text{C}_3=\text{C}_4-\text{C}_5-\text{C}_6-\text{C}_7
  • • The first double bond is between C1 and C2.
  • • The second double bond is between C3 and C4.
  • • They are separated by a single σ bond between C2 and C3.
  • • Thus, hepta-1,3-diene contains conjugated double bonds.
Step 3

Analyze the Other Compounds

1. hepta-1,4-diene: CH₂=CH-CH₂-CH=CH-CH₂-CH₃ (separated by one -CH₂- group; isolated). 2. hepta-1,5-diene: CH₂=CH-CH₂-CH₂-CH=CH-CH₃ (separated by two -CH₂- groups; isolated). 3. hepta-1,6-diene: CH₂=CH-CH₂-CH₂-CH₂-CH=CH₂ (separated by three -CH₂- groups; isolated).

Only hepta-1,3-diene is conjugated (Option 1)\text{Only hepta-1,3-diene is conjugated (Option 1)}
  • • Matches Option (1).
⭐

360° Option Elimination Engine Key Feature

Diagnose every choice: Know exactly why the right option works and why distractors fail.

4-Option Deep Scan
1 A
✓ 100% Correct
Verdict & Scientific Reason:

Exact match with the definition of a conjugated diene (alternating double and single bonds).

💡
Why this is airtight: None; elementary organic principle.
2 B
✗ Incorrect
Verdict & Scientific Reason:

Incorrect. An isolated diene with an intervening sp³ methylene bridge.

⚠️
Student Fallacy (Why candidates pick this trap): Thinking a single methylene group allows conjugation.
3 C
✗ Incorrect
Verdict & Scientific Reason:

Incorrect. Isolated diene with two intervening methylene groups.

⚠️
Student Fallacy (Why candidates pick this trap): Misunderstanding the term conjugated.
4 D
✗ Incorrect
Verdict & Scientific Reason:

Incorrect. Terminal isolated diene with three intervening methylene groups.

⚠️
Student Fallacy (Why candidates pick this trap): Confusing terminal double bonds with conjugated double bonds.
⚠️

NTA Trap Alert: Confusing Cumulated, Conjugated, and Isolated Dienes

Students occasionally mix up conjugated (1,3-diene) with isolated (1,4-diene). Conjugation REQUIRES p-orbital overlap across adjacent carbons without an intervening sp³ spacer.

🛡️ How to avoid the -1 mark: Locants 1,3 = Conjugated; Locants 1,2 = Cumulated; Locants 1,4 or greater = Isolated.
📖

Core NEET Syllabus Standard

NEET Chemistry Core Syllabus · General Organic Chemistry Standard Benchmark
Core Scientific Principle Tested:

"A conjugated system consists of alternating single and multiple bonds."

Syllabus Focus: Classification of hydrocarbons, resonance, and conjugated systems
✓ Core NEET UG Syllabus Anchor Syllabus & Academic Standards ↗
1 and 3 are side-by-side conjugated glee; 1 and 4 are isolated at sea!

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