Q.Give the IUPAC names of the following compounds:
Concept understanding — Structural Isomerism
Structural Isomerism: The First Meeting
Imagine you have a box of identical Lego bricks — four red, ten blue, and six yellow. You build two different models: a car and a house. Both use exactly the same number of each colour brick, but the structures are completely different. That is the core idea of isomerism: same atoms, different arrangement.
In chemistry, molecules are not just a list of atoms. How those atoms are connected matters enormously. Two molecules can have the exact same molecular formula (same number of each atom) but be connected in different ways. Those are structural isomers (also called constitutional isomers).
The Precise Statement
Structural isomers are compounds that have the same molecular formula but different connectivity of atoms — that is, different structural formulas.
The key word is connectivity. Which atom is bonded to which? If you change that, you get a different substance with different physical and chemical properties.
A Concrete Example: C₄H₁₀
Take butane, C₄H₁₀. There are exactly two ways to connect four carbon atoms and ten hydrogen atoms:
- n-Butane — a straight chain: C–C–C–C
- Isobutane (2-methylpropane) — a branched chain: a central carbon bonded to three methyl groups
Both have formula C₄H₁₀. But n-butane boils at –0.5 °C, while isobutane boils at –11.7 °C. Same atoms, different connectivity → different substance.
Structural isomers are not the same molecule. They are distinct compounds that happen to share a molecular formula. You cannot rotate or flip one to get the other — you must break and reform bonds.
The Three Main Types
Structural isomerism comes in three flavours:
| Type | What changes | Example (C₃H₆O) |
|---|---|---|
| Chain isomerism | The carbon skeleton (straight vs. branched) | Butane vs. isobutane |
| Position isomerism | The location of a functional group or substituent | Propan-1-ol vs. propan-2-ol (OH on carbon 1 vs. carbon 2) |
| Functional group isomerism | The atoms are rearranged into a different functional group | Propanal (aldehyde) vs. propanone (ketone) — both C₃H₆O |
Do not confuse structural isomers with stereoisomers. Stereoisomers have the same connectivity but differ in spatial arrangement (like left and right hands). That is a completely different chapter. For now: structural isomers = different bond connections.
Why This Matters
Structural isomers can have wildly different properties. Ethanol (C₂H₆O) is a drinkable alcohol; its isomer dimethyl ether is a gas used as a refrigerant. Same atoms, but one is a liquid you can consume, the other is a gas that would kill you. That is why chemists care so much about connectivity — it determines everything.
Quick Check
Question: Are these structural isomers?
Molecule A: CH₃–CH₂–CH₂–CH₃
Molecule B: CH₃–CH(CH₃)–CH₃
Answer: Yes. Both are C₄H₁₀. A is n-butane (straight chain), B is isobutane (branched). Different connectivity → structural isomers.
The molecular formula must be identical. If the formulas differ, they are not isomers at all — just different compounds.
Structural isomerism is introduced in the NCERT/CBSE Class 11 Chemistry chapter on Organic Chemistry: Some Basic Principles and Techniques, and ‘structural isomerism examples class 11’ is a frequently searched important-question topic for board exams, JEE Main and NEET. Correctly distinguishing structural isomers by connectivity, rather than just matching molecular formulas, is a skill tested throughout competitive organic chemistry exams.
Why this formula?
Structural Isomerism: Why the Key Ideas Hold
Structural isomerism arises when molecules share the same molecular formula but differ in the connectivity of atoms. There is no single "formula" for structural isomerism — instead, the key is understanding why different arrangements are possible.
The Core Principle: Connectivity ≠ Composition
A molecular formula tells you how many of each atom are present, but not how they are joined. Structural isomers exist because atoms can form bonds in multiple distinct sequences while satisfying valency rules.
Why This Happens: The Valency Constraint
Each atom has a fixed bonding capacity (valency):
- Carbon: 4 bonds
- Hydrogen: 1 bond
- Oxygen: 2 bonds
- Nitrogen: 3 bonds
Example: For C4H10, the formula satisfies 4(4)+10(1)=26 valence electrons. But the carbon atoms can be arranged as:
- A straight chain: CH3−CH2−CH2−CH3 (n-butane)
- A branched chain: CH3−CH(CH3)−CH3 (isobutane)
Both satisfy valency, but the connectivity differs.
The "Formula" for Counting Isomers: Why It's Not Simple
There is no closed-form formula to count structural isomers for a given molecular formula. The number grows rapidly and depends on:
- Carbon skeleton branching possibilities
- Functional group positions
- Ring formation possibilities
Why No Simple Formula Exists
The problem is combinatorial — the number of possible trees (acyclic graphs) with n carbon atoms grows exponentially. For example:
- C4H10: 2 structural isomers
- C5H12: 3 structural isomers
- C6H14: 5 structural isomers
- C10H22: 75 structural isomers
The pattern follows Cayley's formula for trees, but even that counts only carbon skeletons — not functional group positions.
Key Reasoning: The Branching Principle
The fundamental reason structural isomers exist is that carbon chains can branch. Consider C5H12:
- Straight chain: C−C−C−C−C (n-pentane)
- One branch: C−C−C(C)−C (isopentane) — the branch can be at position 2 or 3, but these are identical due to symmetry
- Two branches: C−C(C)(C)−C (neopentane) — a quaternary carbon
Why position matters: The branch location changes the carbon's environment, altering physical and chemical properties.
The Functional Group Position Rule
For compounds with functional groups (e.g., alcohols CnH2n+2O), the position of the -OH group creates isomers:
- CH3CH2CH2OH (propan-1-ol) — OH at end
- CH3CH(OH)CH3 (propan-2-ol) — OH in middle
Why these are distinct: The OH group's position changes the carbon's hybridization environment and the molecule's polarity.
The Ring-Chain Isomerism Reason
For unsaturated formulas like C4H8, the same formula can represent:
- A straight alkene: CH2=CH−CH2−CH3
- A branched alkene: CH3−C(=CH2)−CH3
- A cycloalkane: cyclobutane (ring)
Why rings form: Carbon atoms can bond to form closed loops, reducing the number of hydrogen atoms needed. The formula CnH2n can be either an alkene (one double bond) or a cycloalkane (one ring).
Summary: The Takeaway
| Aspect | Why It Holds |
|---|---|
| Different connectivity | Atoms can bond in multiple sequences while satisfying valency |
| No simple counting formula | The number of possible trees grows combinatorially |
| Branching creates isomers | Carbon chains can have branches at different positions |
| Position matters | Functional groups at different locations change properties |
| Rings vs. chains | Same formula can represent open chains or closed rings |
The key insight: Structural isomerism exists because molecular formula is a constraint, not a blueprint — it tells you the ingredients, not the recipe.
Concept: Structural Isomerism & IUPAC Nomenclature – The key is to identify the longest carbon chain, number it to give the lowest locants to substituents (using the alphabetical tiebreak when two numbering directions give the same locant set), and name substituents alphabetically (ignoring multiplying prefixes like di, tri).
(i) CH3CH(Cl)CH(Br)CH3
Longest chain is 4 carbons (butane). The locant set {2,3} is the same from either end, so the alphabetical tiebreak decides: bromo outranks chloro, so bromo gets the lower locant.
2-Bromo-3-chlorobutane
(ii) CHF2CBrClF
Two-carbon chain (ethane). Substituents: F, Cl, Br on C1; two F on C2. Alphabetical order: bromo, chloro, difluoro.
1-Bromo-1-chloro-1,2,2-trifluoroethane
(iii) ClCH2C≡CCH2Br
Four-carbon chain with a triple bond (but-2-yne). The locant set {1,4} is tied either way, so the alphabetical tiebreak applies again: bromo outranks chloro.
1-Bromo-4-chlorobut-2-yne
(iv) (CCl3)3CCl
The longest chain runs THROUGH the central carbon and into TWO of its three trichloromethyl branches at once (a genuine 3-carbon chain), leaving the third CCl₃ as a trichloromethyl substituent and the remaining Cl as a plain chloro substituent on the middle carbon. All 7 chain chlorines (3 + 1 + 3) are cited together under one prefix.
1,1,1,2,3,3,3-Heptachloro-2-(trichloromethyl)propane
(v) CH3C(p-ClC6H4)2CH(Br)CH3
Longest chain: 4 carbons (butane). Numbering from the end nearer the two aryl groups gives locant set {2,2,3}, which beats the flipped {2,3,3} at the first point of difference.
3-Bromo-2,2-bis(4-chlorophenyl)butane
(vi) (CH3)3CCH=CClC6H4I-p
The longest chain absorbs ONE of the tert-butyl group's three methyls (methyl–C–CH=CCl, 4 carbons), leaving the other two methyls as substituents on C-3. Numbered from the C=CCl end so the double bond gets the lowest locant (1, not 3).
1-Chloro-1-(4-iodophenyl)-3,3-dimethylbut-1-ene
- 2-Bromo-3-chlorobutane,
- 1-Bromo-1-chloro-1,2,2-trifluoroethane,
- 1-Bromo-4-chlorobut-2-yne,
- 1,1,1,2,3,3,3-Heptachloro-2-(trichloromethyl)propane,
- 3-Bromo-2,2-bis(4-chlorophenyl)butane,
- 1-Chloro-1-(4-iodophenyl)-3,3-dimethylbut-1-ene.
Applying the longest-chain / lowest-locant / alphabetical rules: (i) 2-bromo-3-chlorobutane,
(ii) 1-bromo-1-chloro-1,2,2-trifluoroethane,
(iii) 1-bromo-4-chlorobut-2-yne,
(iv) 1,1,1,2,3,3,3-heptachloro-2-(trichloromethyl)propane,
(v) 3-bromo-2,2-bis(4-chlorophenyl)butane,
(vi) 1-chloro-1-(4-iodophenyl)-3,3-dimethylbut-1-ene.
(i) CH3CH(Cl)CH(Br)CH3 - parent butane; Br and Cl fall on C2/C3 either way (locants tie), so the alphabetically-first substituent (bromo) takes the lower number -> 2-bromo-3-chlorobutane.
(ii) CHF2CBrClF - parent ethane; numbering from the CBrClF end gives the lower locant set {1,1,1,2,2} (vs {1,1,2,2,2}) -> 1-bromo-1-chloro-1,2,2-trifluoroethane.
(iii) ClCH2C≡CCH2Br - parent but-2-yne; substituent locants {1,4} tie, so bromo takes position 1 -> 1-bromo-4-chlorobut-2-yne.
(iv) (CCl3)3CCl - the longest chain runs through the central carbon between two CCl3 groups, giving a propane parent; C1 and C3 each carry three Cl, the central C2 carries one Cl plus the third CCl3 as a (trichloromethyl) substituent -> 1,1,1,2,3,3,3-heptachloro-2-(trichloromethyl)propane.
(v) CH3C(p-ClC6H4)2CH(Br)CH3 - parent butane; numbering with the two aryl groups at C2 gives the locant set {2,2,3} (aryl, aryl, bromo), which beats numbering the other way with Br at C2 ({2,3,3}) at the first point of difference (2 < 3) -> 3-bromo-2,2-bis(4-chlorophenyl)butane. (The alphabetical rule only breaks a TRUE tie in the locant set -- here the sets themselves already differ, so the lower-locant-set rule decides first.)
(vi) (CH3)3CCH=CClC6H4I-p - the longest chain through the C=C includes one methyl of the tert-butyl group, giving a four-carbon but-1-ene chain; numbering from the doubly-bonded end that bears Cl and the aryl group -> 1-chloro-1-(4-iodophenyl)-3,3-dimethylbut-1-ene.
- 2-bromo-3-chlorobutane;
- 1-bromo-1-chloro-1,2,2-trifluoroethane;
- 1-bromo-4-chlorobut-2-yne;
- 1,1,1,2,3,3,3-heptachloro-2-(trichloromethyl)propane;
- 3-bromo-2,2-bis(4-chlorophenyl)butane;
- 1-chloro-1-(4-iodophenyl)-3,3-dimethylbut-1-ene.
Structural Isomerism — IUPAC Naming Method
Method: Systematic IUPAC Nomenclature (Substitutive Naming)
This method follows the IUPAC Blue Book rules: identify the longest parent chain, number it to give lowest locants to substituents (breaking ties alphabetically when two numbering directions give the same locant set), name substituents alphabetically, and specify multiple bonds where present.
Steps for each compound:
- Identify the longest carbon chain (parent alkane/alkene/alkyne) — check every direction a chain can run, including through a branch point in more than one direction.
- Number the chain to give the lowest possible locants to substituents; if tied, the substituent cited first alphabetically gets the lower locant.
- Name substituents (halogens, alkyl groups, etc.) in alphabetical order.
- Specify multiple bonds with appropriate suffixes (-ene, -yne), giving them priority for low locants.
- Combine identical substituents under one multiplying prefix, citing all their locants together.
Solutions
(i) CH3CH(Cl)CH(Br)CH3
- Parent chain: 4 carbons → butane
- Locant set for the two substituents is {2,3} from either end (symmetric chain) — the alphabetical tiebreak applies: bromo (b) outranks chloro (c), so bromo gets the lower locant.
Answer: 2-bromo-3-chlorobutane
(ii) CHF2CBrClF
- Parent chain: 2 carbons → ethane
- Substituents: F (×2) at C-1, Br, Cl, F at C-2
- Alphabetical: bromo, chloro, difluoro
Answer: 1-bromo-1-chloro-1,2,2-trifluoroethane
(iii) ClCH2C≡CCH2Br
- Parent chain: 4 carbons with triple bond → but-2-yne
- Locant set {1,4} tied either way — alphabetical tiebreak: bromo before chloro, so bromo gets locant 1.
Answer: 1-bromo-4-chlorobut-2-yne
(iv) (CCl3)3CCl
- The central carbon is bonded to Cl and three CCl₃ groups. The longest chain does not stop at the centre — it runs through the centre and into two of the three CCl₃ branches at once, giving a genuine 3-carbon chain (propane), with the third CCl₃ left over as a substituent.
- C-1 and C-3: three chlorines each (from their own CCl₃ origin). C-2 (the original centre): one chlorine + one trichloromethyl branch.
- All 7 chain chlorines (3 + 1 + 3, at locants 1,1,1,2,3,3,3) are cited together as heptachloro.
Answer: 1,1,1,2,3,3,3-heptachloro-2-(trichloromethyl)propane
(v) CH3C(p-ClC6H4)2CH(Br)CH3
- Parent chain: 4 carbons → butane
- Numbering from the end nearer the two aryl groups gives locant set {2,2,3} for (aryl, aryl, bromo) — lower than the flipped {2,3,3} at the first point of difference.
- Substituents: two 4-chlorophenyl groups at C-2, bromo at C-3
- Alphabetical: bromo, chlorophenyl
Answer: 3-bromo-2,2-bis(4-chlorophenyl)butane
(vi) (CH3)3CCH=CClC6H4I-p
- The longest chain is NOT the tert-butyl group treated as an intact substituent on a short chain — it absorbs one of the tert-butyl's three methyls into the chain itself: methyl–C–CH=CCl, 4 carbons (but-1-ene), leaving the other two methyls as substituents on C-3.
- Numbering must start from the C=CCl end so the double bond gets locant 1 (not 3) — the double bond outranks ordinary substituents for low-locant priority.
- Substituents: chloro and 4-iodophenyl at C-1, two methyl at C-3.
- Alphabetical: chloro, iodophenyl, methyl
Answer: 1-chloro-1-(4-iodophenyl)-3,3-dimethylbut-1-ene
Key exam tip: Always check for the lowest locant set first — if two numbering directions give the same set, only then compare alphabetically. And always check whether the "obvious" chain (e.g. treating a tert-butyl or CCl₃ group as a fixed substituent) is really the LONGEST one — a chain can run through a branch point in more than one direction.
This is a classic area where even good students lose marks. Let's go compound by compound, listing the common mistakes and how to avoid each.
(i) CH3CH(Cl)CH(Br)CH3
✗ Common Mistakes
- Wrong parent chain selection — students sometimes number from the wrong end, giving a higher locant sum.
- Alphabetical tiebreak applied backwards — writing "chlorobromo" or defaulting to whichever halogen is drawn first, instead of checking which one is alphabetically first.
- Missing commas and hyphens — e.g.,
2-chloro 3-bromobutaneinstead of the correctly punctuated name.
✓ How to Avoid
- Find the longest carbon chain — here it's 4 carbons (butane).
- Check the locant set first — both Cl and Br sit at positions 2 and 3 regardless of which end you number from, so the locant SET is tied at {2,3}.
- Break the tie alphabetically — the substituent cited first alphabetically (bromo, "b") gets the lower locant, not chloro.
- Write substituents in alphabetical order (ignoring di-, tri- prefixes for alphabetizing).
Correct IUPAC name:
2-bromo-3-chlorobutane
(ii) CHF2CBrClF
✗ Common Mistakes
- Not recognizing this is a haloalkane with multiple different halogens — students often misorder the substituents.
- Wrong parent chain — some pick a 1-carbon chain instead of 2-carbon (ethane).
- Alphabetizing "difluoro" by its "d" rather than remembering that a simple multiplying prefix (di-, tri-) is normally ignored for alphabetization — except that here it doesn't matter, since "difluoro" and "fluoro" both alphabetize as "fluoro" and are tied with each other, not with bromo/chloro.
✓ How to Avoid
- Identify the longest carbon chain — 2 carbons → ethane.
- Number the chain so that substituents get the lowest locants. Comparing the two numbering directions, the one that puts three chlorine-family substituents (Br, Cl, F) on C-1 and both remaining F's on C-2 gives the lower locant set — so C1 = CBrClF, C2 = CHF₂.
- List substituents alphabetically — bromo, chloro, difluoro.
Correct IUPAC name:
1-bromo-1-chloro-1,2,2-trifluoroethane
(iii) ClCH2C≡CCH2Br
✗ Common Mistakes
- Not recognizing the triple bond — students sometimes treat it as an alkane.
- Miscounting the parent chain length — this is a common trap: there are only 4 carbons here (but-2-yne), not 5 — don't count a substituent atom (Cl or Br) as if it were a chain carbon.
- Alphabetical tiebreak applied backwards — same trap as compound (i): the locant set {1,4} is tied either way, so bromo (alphabetically first) must get the lower locant.
✓ How to Avoid
- Identify the functional group — triple bond (alkyne). Parent chain must include it.
- Count only carbon atoms in the chain — Cl–CH₂–C≡C–CH₂–Br has exactly 4 carbons → but-2-yne.
- Break the tied locant set alphabetically — bromo before chloro, so bromo gets locant 1.
Correct IUPAC name:
1-bromo-4-chlorobut-2-yne
(iv) (CCl3)3CCl
✗ Common Mistakes
- Stopping the chain at the central carbon — students often name this as a substituted methane (with three "trichloromethyl" branches), missing that the chain can run straight THROUGH the centre and into two of the branches at once.
- Splitting identical substituents into separate citations — e.g. writing "2-chloro...hexachloro..." as two separate chlorine citations instead of combining every chain chlorine under one multiplying prefix.
✓ How to Avoid
- Draw the structure — central C bonded to Cl and three CCl₃ groups.
- Look for a chain that passes through the branch point — going from one CCl₃'s carbon, through the centre, into a second CCl₃'s carbon gives a genuine 3-carbon chain (propane). This beats stopping at 1 carbon (methane).
- The third CCl₃ becomes a substituent — named "trichloromethyl" — and the Cl on the (now middle) chain carbon is a plain chloro substituent.
- Combine every identical substituent — all 7 chain chlorines (three from each end carbon, one from the middle) are cited together as heptachloro with all their locants listed.
Correct IUPAC name:
1,1,1,2,3,3,3-heptachloro-2-(trichloromethyl)propane
(v) CH3C(p-ClC6H4)2CH(Br)CH3
✗ Common Mistakes
- Not recognizing the aromatic rings — students forget to name the p-chlorophenyl groups.
- Numbering from the wrong end — giving bromo locant 2 and the aryl groups locant 3, instead of checking which direction actually gives the lower locant SET.
✓ How to Avoid
- Identify the longest carbon chain — 4 carbons (butane). The two aromatic rings are substituents, not chain extensions (each aryl ring attaches by a single bond, it isn't a continuation of the carbon chain).
- Compare both numbering directions — locants {aryl, aryl, bromo} = {2,2,3} from one end vs {2,3,3} from the other. {2,2,3} is lower at the first point of difference.
- Alphabetical order — bromo, then chlorophenyl (since "b" < "c"). Use "bis" for two identical aryl groups.
Correct IUPAC name:
3-bromo-2,2-bis(4-chlorophenyl)butane
(vi) (CH3)3CCH=CClC6H4I-p
✗ Common Mistakes
- Treating "tert-butyl" as a fixed, intact substituent — this hides a longer chain: one of the tert-butyl's three methyls can be absorbed into the main chain itself, since it's directly bonded to the chain carbon.
- Numbering the double bond from the wrong end — a double bond gets priority for the lowest possible locant, so the chain must be numbered starting from the C=CCl end, not from the tert-butyl end.
✓ How to Avoid
- Look for a longer chain through the "obvious" substituent — methyl–C(CH₃)₂–CH=CCl– is a genuine 4-carbon chain (but-1-ene) once one methyl of the tert-butyl group is counted as part of the chain; the other two methyls remain as substituents.
- Give the double bond the lowest locant — numbering from the C=CCl end puts it at C-1, not C-3.
- Substituents — chloro and 4-iodophenyl both on C-1, two methyl groups on C-3.
- Alphabetical order — chloro, iodophenyl, methyl.
Correct IUPAC name:
1-chloro-1-(4-iodophenyl)-3,3-dimethylbut-1-ene
Summary Table of Key Mistakes
| Compound | Common Mistake | How to Avoid |
|---|---|---|
| (i) | Alphabetical tiebreak applied backwards | When the locant set is tied, the alphabetically-first substituent gets the lower locant |
| (ii) | Wrong parent chain | Always find longest C chain |
| (iii) | Miscounting chain length / backwards tiebreak | Count only carbon atoms; apply the same alphabetical tiebreak rule |
| (iv) | Stopping the chain at the branch point | Check whether the chain can run through the branch point into two arms at once |
| (v) | Numbering from the wrong end | Compare BOTH numbering directions' full locant sets before choosing |
| (vi) | Treating a common group name (tert-butyl) as fixed | A "named group" can still be split if that gives a longer chain |
Final tip: Always draw the structure first, then apply IUPAC rules step-by-step — longest chain (checking every direction, including through branch points) → numbering (lowest locant set, alphabetical tiebreak) → substituents combined and alphabetized. This eliminates most errors.
Showing the 12 most recent of 17 on this concept.
- CBSE 2026Set DZ1 markMCQQ.Which of the following is an aldehyde?(a) CH3−C∣∣O−H(b) CH3−CH2−C∣∣O−CH3(c) CH3−CH2−C∣∣O−CH2−CH3(d) CH3−C∣∣O−CH3
›Reveal solutionSolution
An aldehyde has the −CHO group (a carbonyl carbon bonded to at least one H). Only option (a) has this; the rest are ketones.
The functional-group test: in an aldehyde the carbonyl carbon (>C=O) carries at least one hydrogen (R−CHO). In a ketone the carbonyl carbon is bonded to two carbon atoms (R−CO−R′).
-
(a) CH3−CHO → carbonyl C bonded to one H → aldehyde (ethanal) ✓
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(b) CH3CH2−CO−CH3 → butan-2-one → ketone
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(c) CH3CH2−CO−CH2CH3 → pentan-3-one → ketone
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(d) CH3−CO−CH3 → propanone (acetone) → ketone
✓Final answer(a) CH3CHO (acetaldehyde/ethanal).
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- CBSE 2026Set A1 markMCQQ.Which of the following is Isopropyl amine ?(a) CH3-CH2-CH2-NH2(b) CH3-NH-C2H5(c) CH3-CH(NH2)-CH3(d) CH3-CH(CH3)-CH2-NH2
›Reveal solutionSolution
Isopropyl amine = propan-2-amine, CH3-CH(NH2)-CH3.
The isopropyl group is (CH3)2CH-, so isopropylamine has the amino group attached to the central carbon of a propane chain: CH3-CH(NH2)-CH3 (propan-2-amine). For reference:
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(a) CH3-CH2-CH2-NH2 is n-propylamine (propan-1-amine)
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(b) CH3-NH-C2H5 is N-methylethylamine (a secondary amine)
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(d) is isobutylamine
✓Final answer(c) CH3-CH(NH2)-CH3.
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- CBSE 2026Set ANNUAL1 markQ.How many structural isomers of C5H11Br are possible?
›Reveal solutionSolution
C5H11Br has 8 possible structural isomers, arising from bromine substitution at different positions on the three possible pentane carbon skeletons.
C5H11Br is derived from pentane (C5H12) by replacing one H with Br. Pentane itself has 3 carbon-skeleton isomers, and Br can go on different, non-equivalent carbon positions of each:
From n-pentane skeleton (CH3CH2CH2CH2CH3):
- 1-bromopentane
- 2-bromopentane
- 3-bromopentane (C4 and C5 positions are equivalent to C2 and C1 by the molecule's symmetry)
From isopentane / 2-methylbutane skeleton ((CH3)2CHCH2CH3):
4. 1-bromo-2-methylbutane
5. 2-bromo-2-methylbutane
6. 3-bromo-2-methylbutane
7. 1-bromo-3-methylbutane (isoamyl bromide)
From neopentane / 2,2-dimethylpropane skeleton ((CH3)3CCH3, i.e. (CH3)4C):
8. Neopentyl bromide (1-bromo-2,2-dimethylpropane)
Of these 8: 4 are primary bromides, 3 are secondary, and 1 is tertiary.
✓Final answer8 structural isomers.
- CBSE 2026Set ANNUAL1 markMCQQ.Ethylidine dichloride is a:(a) vic-dihalide(b) gem-dihalide(c) allylic dihalide(d) vinylic halide
›Reveal solutionSolution
Ethylidene dichloride, CH₃CHCl₂, has both chlorine atoms on the same carbon — a gem-dihalide.
Ethylidene dichloride has the structure CH₃–CHCl₂. Both chlorine atoms are attached to the same carbon atom (the second carbon). Dihalides in which both halogens sit on one carbon are called geminal (gem) dihalides; when they are on adjacent carbons they are called vicinal (vic) dihalides. Since both Cl atoms here are on one carbon, this is a gem-dihalide.
✓Final answer(b) gem-dihalide.
- CBSE 2026Set ANNUAL1 markMCQQ.The correct IUPAC name of the organic compound CH₃—CH(C₂H₅)—CH₂Br is-(a)(i) 1-Bromo-2-ethyl-2 methyl ethane(b)(ii) 1-Bromo-2-ethyl propane(c)(iii) 1-Bromo-2-methyl butane(d)(iv) 2-Methyl-1-bromo butane
›Reveal solutionSolution
CH3–CH(C2H5)–CH2Br names as 1-bromo-2-methylbutane. Correct option: (iii).
Concept. IUPAC naming of a haloalkane: (1) pick the longest carbon chain that contains the carbon bearing the halogen; (2) number so the substituents get the lowest set of locants; (3) cite substituents alphabetically as prefixes.
Steps.
- The structure is BrCH2–CH(CH3)–CH2–CH3.
- Longest chain through the C–Br carbon = 4 carbons (butane): C1(CH2Br)−C2(CH)−C3(CH2)−C4(CH3).
- Number from the Br end: bromo at C-1, methyl branch at C-2.
- Name: 1-bromo-2-methylbutane.
Why other options are wrong. (i) and (ii) use "ethane/propane" as the parent — they fail to select the longest chain (butane). (iv) "2-methyl-1-bromobutane" mis-orders the substituents (alphabetical order requires bromo before methyl).
✓Final answer(iii) 1-Bromo-2-methylbutane. This IUPAC nomenclature is common to the NCERT/CBSE-aligned UBSE Class-12 Chemistry course.
- CBSE 2025Set JZ1 markMCQQ.The correct IUPAC name for CH2=CHCH2NHCH3 is :(a) Allylmethylamine(b) 1-amine-4-pentene(c) 4-aminopent-1-ene(d) N-methylprop-2-ene-1-amine
›Reveal solutionSolution
Naming CH2=CHCH2NHCH3 as a substituted amine gives N-methylprop-2-en-1-amine — option (d).
Concept. For a secondary amine, choose the longest carbon chain attached to nitrogen as the parent amine; the smaller alkyl group on N is named as an N-substituent.
Working:
- Parent chain: CH2=CH−CH2− is a 3-carbon chain with a double bond → prop-2-ene; the amino group is on C-1 → prop-2-en-1-amine.
- The nitrogen also carries a −CH3, written as the prefix N-methyl.
Combining: N-methylprop-2-en-1-amine (the common name is allylmethylamine, but the IUPAC name is required).
✓Final answer(d) N-methylprop-2-ene-1-amine.
- CBSE 2025Set D1 markMCQQ.The number of isomeric alcohols of molecular formula C4H10O is(a) 2(b) 4(c) 7(d) 8
›Reveal solutionSolution
The four alcohols of formula C4H10O are 1-butanol, 2-methyl-1-propanol, 2-butanol and 2-methyl-2-propanol.
For the molecular formula C4H10O with an -OH group, the possible alcohols are:
- n-Butanol (butan-1-ol): CH3CH2CH2CH2OH (1°)
- Isobutyl alcohol (2-methylpropan-1-ol): (CH3)2CHCH2OH (1°)
- sec-Butyl alcohol (butan-2-ol): CH3CH2CH(OH)CH3 (2°)
- tert-Butyl alcohol (2-methylpropan-2-ol): (CH3)3COH (3°)
That gives 4 isomeric alcohols. (The remaining C4H10O isomers such as diethyl ether are ethers, not alcohols.)
✓Final answer(B) 4 isomeric alcohols of formula C4H10O.
- CBSE 2025Set ANNUAL1 markMCQQ.The number of isomers in C2BrClFI is(a) 3(b) 4(c) 5(d) 6
›Reveal solutionSolution
C2BrClFI, an ethylene bearing all four halogens (Br, Cl, F, I) with no hydrogens, has 6 possible isomers.
Since the formula has 2 carbons and exactly 4 substituents (Br, Cl, F, I) with no hydrogens, this corresponds to a fully-substituted ethylene, i.e. an alkene of type (X)(Y)C=C(Z)(W), where each carbon bears 2 of the 4 different halogens.
Step 1 — constitutional (positional) isomers: choose which 2 of the 4 halogens sit on one carbon (the other 2 automatically go on the other carbon). The number of distinct ways to split 4 different halogens into two unordered pairs is 3: {Br,Cl}|{F,I}, {Br,F}|{Cl,I}, {Br,I}|{Cl,F}.
Step 2 — geometric (cis/trans) isomers: for each of these 3 constitutional arrangements, since each carbon carries 2 different substituents, the molecule can exist as 2 geometric isomers (cis and trans, i.e. Z and E).
Total isomers = 3 (constitutional arrangements) x 2 (geometric isomers each) = 6.
✓Final answer(D) 6.
- CBSE 2024Set ANNUAL1 markMCQQ.An isomer of ethanol is(a) Methanol(b) Dimethyl ether(c) Diethyl ether(d) Ethylene glycol
›Reveal solutionSolution
Dimethyl ether (CH3–O–CH3) is the classic functional isomer of ethanol (C2H6O).
Ethanol (CH3CH2OH) has molecular formula C2H6O. Dimethyl ether (CH3–O–CH3) has the identical molecular formula C2H6O but a completely different functional group (ether linkage instead of an –OH group) — this is an example of functional group isomerism. Methanol (CH4O) and diethyl ether (C4H10O) have different molecular formulas, so they are not isomers of ethanol; ethylene glycol (C2H6O2) also has a different formula.
✓Final answer(B) Dimethyl ether.
- CBSE 2024Set ANNUAL1 markMCQQ.The total number of isomers for the compounds having molecular formula C4H10O is(a) 7(b) 6(c) 3(d) 4
›Reveal solutionSolution
C4H10O has 7 total structural isomers: 4 alcohols + 3 ethers.
Alcohols (C4H9OH, 4 isomers): butan-1-ol, butan-2-ol, 2-methylpropan-1-ol (isobutanol), 2-methylpropan-2-ol (tert-butanol).
Ethers (C4H10O, 3 isomers): diethyl ether (C2H5–O–C2H5), methyl n-propyl ether (CH3–O–CH2CH2CH3), methyl isopropyl ether (CH3–O–CH(CH3)2).
Total = 4 + 3 = 7 constitutional isomers.
✓Final answer(A) 7.
- CBSE 2023Set ANNUAL1 markQ.How many isomeric monochloro derivatives will be formed when 2-methylpropane is subjected to photochlorination ?
›Reveal solutionSolution
2-Methylpropane has only two chemically distinct kinds of hydrogen (9 equivalent primary H's and 1 tertiary H), so free-radical photochlorination gives exactly two monochloro isomers.
2-Methylpropane (isobutane), (CH3)3CH, has two types of hydrogen atoms:
- 9 primary hydrogens (three equivalent CH3 groups), all chemically equivalent by symmetry — substitution at any of these gives the same product: 1-chloro-2-methylpropane, (CH3)2CHCH2Cl.
- 1 tertiary hydrogen (on the central carbon) — substitution here gives: 2-chloro-2-methylpropane (tert-butyl chloride), (CH3)3CCl.
Since photochlorination is a free-radical substitution that can occur at any C–H bond, but chemically equivalent hydrogens always give the identical product, the number of distinct isomeric monochloro products depends only on the number of structurally different types of hydrogen, not the total count of hydrogens.
✓Final answer2 isomeric monochloro derivatives: 1-chloro-2-methylpropane (from the primary H's) and 2-chloro-2-methylpropane / tert-butyl chloride (from the tertiary H).
- CBSE 2023Set ANNUAL1 markMCQQ.CH2=CH-CH2-CH3 and CH3-CH=CH-CH3 are:(a) Chain isomers(b) Position isomers(c) Functional isomers(d) Metamers
›Reveal solutionSolution
CH2=CH-CH2-CH3 (1-butene) and CH3-CH=CH-CH3 (2-butene) share the same carbon skeleton and functional group but differ only in where the double bond sits — that is positional isomerism.
Both molecules have molecular formula C4H8 and the same unbranched 4-carbon chain, and both are alkenes (same functional group, so not functional isomers; same chain, so not chain isomers).
The only difference is the location of the C=C double bond: between C1–C2 in the first compound (1-butene) versus between C2–C3 in the second (2-butene). This difference in position of the double bond (or functional group) along an otherwise identical skeleton defines position isomers.
✓Final answerPosition isomers (option b).
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