Q.Which of the following compounds will give racemic mixture on nucleophilic substitution by OH− ion?
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🔒 Start your 14-day free trial to unlock the full solution →Concept understanding — SN1 Reactivity Order
The Core Intuition: Who Wants to Leave, and Who Can Wait?
Imagine you're at a party where the host (the leaving group) is about to leave. The party (the reaction) happens in two stages. First, the host walks out the door — that's the slow, painful step. Then, a new guest (the nucleophile) rushes in to take the empty spot.
The SN1 reaction works exactly like this: the leaving group leaves first, forming a carbocation intermediate. The nucleophile attacks after the leaving group is gone. This means the rate of the reaction depends only on how easily the leaving group can leave — it does not depend on the nucleophile at all.
So the question becomes: What makes a carbocation form easily? The answer is stability. A carbocation that is more stable will form faster and last longer, making the SN1 reaction faster.
The Precise Statement of SN1 Reactivity Order
SN1 Reactivity Order (for alkyl halides):
Allylic≈Benzyl>3∘>2∘≫1∘≈Methyl
This is the order of how fast the SN1 reaction proceeds. Let's unpack why.
Why This Order? The Stability Ladder
A carbocation is a carbon with only six electrons in its valence shell — it's electron-deficient and positively charged. The more you can spread out (delocalize) that positive charge, the more stable the carbocation becomes.
1. Methyl and 1° Carbocations: The Unstable Ones
A methyl carbocation (CHX3X+) has no alkyl groups attached to the positive carbon. There is zero electron-donating effect to stabilize the charge. It is so unstable that it practically never forms in an SN1 reaction — the reaction simply doesn't happen.
A primary (1°) carbocation has one alkyl group attached. Alkyl groups are weakly electron-donating (through hyperconjugation and inductive effect), so it's slightly more stable than methyl — but still far too unstable to form under normal SN1 conditions.
Never say "SN1 happens on a primary carbon" in an exam. It is essentially impossible under standard conditions because the carbocation is too unstable.
2. Secondary (2°) Carbocations: The Borderline Case
A secondary carbocation has two alkyl groups donating electron density. It is moderately stable — stable enough to form, but only under certain conditions (like a good leaving group and a polar protic solvent). SN1 reactions on secondary carbons are possible, but they are slower than on tertiary carbons.
3. Tertiary (3°) Carbocations: The Sweet Spot
Three alkyl groups donate electron density to the positive carbon. This makes the carbocation very stable. Tertiary alkyl halides undergo SN1 reactions readily — they are the classic example.
4. Allylic and Benzylic: The Champions
These are special cases. In an allylic carbocation, the positive charge is adjacent to a carbon-carbon double bond. The π electrons of the double bond can delocalize the positive charge onto the second carbon:
CHX2=CH−CHX2X+↔+CHX2−CH=CHX2
In a benzylic carbocation, the positive charge is adjacent to a benzene ring. The π system of the ring delocalizes the charge across multiple carbons:
CX6HX5−CHX2X+↔(several resonance structures)
Here are those resonance structures — the positive charge cycles from the CH₂ carbon onto the ortho and para positions of the ring:
This resonance stabilization makes allylic and benzylic carbocations even more stable than tertiary ones. They form the fastest in SN1 reactions.
The Complete Picture in a Table
| Carbocation Type | Stability | SN1 Reactivity | Example |
|------------------|-----------|----------------|---------| …
Why this formula?
SN1 Reactivity Order: Why It Holds
The SN1 reaction (Substitution Nucleophilic Unimolecular) proceeds via a carbocation intermediate. The reactivity order is determined entirely by the stability of this carbocation — because the rate-determining step is its formation.
The Core Principle
The rate law for SN1 is:
Rate=k[RX]
Only the substrate appears in the rate law — the nucleophile does not participate in the slow step. The slow step is:
RXslowR++X−
Thus, anything that stabilizes the carbocation (R⁺) lowers the activation energy and increases the reaction rate.
The Reactivity Order
For alkyl halides (RX), the SN1 reactivity order is:
Allylic>Benzyllic>Tertiary>Secondary>Primary>Methyl
Let's break down why each step holds.
1. Why Tertiary > Secondary > Primary > Methyl?
This is purely about hyperconjugation and inductive effect.
- Tertiary carbocation: Three alkyl groups donate electron density via hyperconjugation (C–H σ bonds overlap with empty p orbital) and +I effect. This spreads the positive charge over more atoms → most stable.
- Secondary: Two alkyl groups → less stabilization.
- Primary: Only one alkyl group → very little stabilization.
- Methyl: No alkyl groups → least stable (only inductive effect from H atoms, which is negligible).
Key formula: The number of α-hydrogens (H on carbons adjacent to the positive carbon) determines hyperconjugation. More α-H → more resonance structures → more stable.
2. Why Allylic and Benzylic Are Even Faster
These carbocations are resonance-stabilized.
- Allylic carbocation: The positive charge is delocalized over two carbon atoms via π-bond conjugation:
CH2=CH−CH2+⟷CH2+−CH=CH2
- Benzylic carbocation: The positive charge is delocalized into the aromatic ring:
C6H5−CH2+⟷several resonance forms involving the ring
Those resonance forms look like this:
This resonance stabilization is so powerful that even a primary allylic or benzylic carbocation is more stable than a tertiary alkyl carbocation.
3. The Complete Order (with reasoning) …
The key idea is that a racemic mixture forms when the reaction proceeds through a planar carbocation intermediate — that is, via an SN1 mechanism. A chiral centre that becomes planar during the reaction will be attacked from either face with equal probability, giving a racemate.
Step 1: Identify the substrate class and check which carbon is actually a stereocentre.
- (a) CH3−CH(Br)−C2H5 is a secondary alkyl halide (2∘). The Br-bearing carbon is attached to CH3, C2H5, H, and Br — four different groups, so it IS a genuine stereocentre.
- (b) CH3−C(Br)(C2H5)−CH3 is a tertiary alkyl halide (3∘). But look at all four groups on the Br-bearing carbon: CH3, CH3, C2H5, Br — two of them are identical methyl groups, so this carbon is not a stereocentre at all, regardless of how easily it ionises.
- (c) CH3−CH(C2H5)−CH2Br does have a genuine stereocentre (the CH carbon bonded to CH3, C2H5, H, CH2Br), but the leaving group Br sits on the adjacent primary CH2Br carbon, not on the stereocentre itself.
Step 2: Determine whether racemisation is actually possible in each case.
- (a): the stereocentre IS the carbon that loses Br. Under conditions with some SN1 character, the resulting planar carbocation can be attacked by OH− from either face, giving both enantiomers — a genuine racemic mixture is possible here. …
A racemic mixture requires the carbon where substitution actually happens to be a genuine stereocentre (four different groups) both before AND after the reaction. Only compound (a)'s reacting carbon qualifies — compound (b)'s reacting carbon carries two identical methyl groups (never a stereocentre at all), and compound (c)'s only stereocentre is a different carbon from the one the bromine leaves. The correct option is (i) — only compound (a).
What "gives a racemic mixture" actually requires
A racemic mixture means two enantiomers of a chiral product forming in equal amounts. That is only possible when the carbon losing the leaving group is itself a genuine stereocentre (four different groups attached) both before the reaction AND in the product — a mechanism with carbocation character (planar intermediate, attackable from either face) is what lets both mirror-image outcomes form.
(a) CH3−CH(Br)−C2H5 (2-bromobutane)
The bromine-bearing carbon is bonded to CH3, C2H5, H, and Br — four different groups, a genuine stereocentre, and this is exactly the carbon where substitution happens. If the mechanism has carbocation character, the resulting planar cation can be attacked from either face, giving both enantiomers of the alcohol product — a real racemic mixture is possible here.
(b) CH3−C(Br)(C2H5)−CH3 (2-bromo-2-methylbutane)
Look carefully at the reacting carbon's four substituents: CH3, CH3, C2H5, Br — two of them are identical methyl groups. This carbon is not a stereocentre at all, either before the reaction or in the product (replacing Br with OH still leaves two identical methyls). Since there is no stereocentre to begin with, "racemic mixture" does not even apply here — attacking the (achiral) carbocation from either face gives the exact same molecule both times, not two enantiomers. …
Method: SN1 Reactivity & Racemisation Check
Step 1 – Recall the condition for racemisation
A racemic mixture forms when the reaction proceeds via an SN1 mechanism — that is, through a planar carbocation intermediate. The nucleophile can attack from either face, giving equal amounts of both enantiomers.
Step 2 – Identify the substrate type
SN1 requires a stable carbocation (tertiary > secondary > primary).
Also, the leaving group must be on a chiral carbon for racemisation to be observed.
Let’s examine each compound:
-
(a) CH3−C2H5∣CH−Br
→ Secondary alkyl halide. Can form a moderately stable carbocation.
→ The carbon bearing Br is chiral (4 different groups: H, CH₃, C₂H₅, Br).
→ SN1 possible → racemic mixture.
-
(b) CH3−C2H5∣C∣Br−CH3
→ Tertiary alkyl halide. Forms a very stable carbocation.
→ The Br-bearing carbon carries CH₃, CH₃, C₂H₅ and Br — two identical methyl groups, so it is not chiral. …
Common Mistakes & How to Avoid Them
Mistake 1: Confusing SN1 with SN2 reactivity
The error: Students assume any alkyl halide with a chiral centre will give a racemic mixture, forgetting that racemic mixture formation is a hallmark of SN1, not SN2.
How to avoid:
- SN1 proceeds via a planar carbocation intermediate → nucleophile attacks from either face → racemic mixture (if the carbon is a stereocentre).
- SN2 proceeds via backside attack → inversion of configuration (no racemisation).
Key rule: Racemic mixture → only if the reacting carbon is a genuine stereocentre AND the mechanism is SN1.
Mistake 2: Assuming a tertiary carbon with a bromine is automatically chiral
The error: Students see compound (b), CH3−C2H5∣C∣Br−CH3, and reason "tertiary carbon, undergoes SN1 easily, so it must give a racemic mixture."
Why it's wrong: Look at ALL FOUR groups on that carbon: CH3, Br, C2H5, and... another CH3. Two of the four groups are identical methyls. A carbon needs four genuinely DIFFERENT groups to be a stereocentre — (b)'s Br-bearing carbon is NOT chiral at all, even though it's tertiary. With no stereocentre to begin with, there's nothing to racemise: the product (2-methylbutan-2-ol) is a single, achiral compound either way, not a "racemic mixture" of two enantiomers.
How to avoid: Before asking "SN1 or SN2," first check: does this carbon actually have four different substituents? Count them explicitly, including any that repeat. If two match, it's not a stereocentre, and the racemisation question doesn't even apply.
Mistake 3: Ignoring the leaving group's position relative to the stereocentre
The error: Students see a chiral carbon elsewhere in the molecule and assume the reaction will affect it, without checking if the leaving group is actually attached to that carbon.
Example from compound (c): CH3−C2H5∣CH−CH2Br — the chiral carbon is the second carbon (bonded to CH3, C2H5, H, and CH2Br — four different groups), but Br sits on the adjacent primary carbon, not on the stereocentre itself.
Why it's wrong: Substitution happens at the primary CH2Br carbon via clean SN2 (fast, no carbocation, and that carbon isn't a stereocentre in the first place). The actual stereocentre is never touched by the reaction — it keeps its original configuration throughout. The product is optically ACTIVE (same single enantiomer as the reactant), not racemic.
How to avoid: Always locate the carbon bearing the leaving group first, and check whether it's the SAME carbon as any stereocentre in the molecule. If the leaving group and the stereocentre are on different carbons, the stereocentre is usually untouched.
Mistake 4: Forgetting to check carbocation stability for compound (a) …
- GSEB Higher Secondary Certificate (HSC) Examination 2026Set ANNUAL1 markMCQQ.For the following compounds, what is the correct increasing order of reactivity towards SN1 displacement? (I) 2-Bromo-2-methylbutane (II) 1-Bromopentane (III) 2-Bromopentane(a) I < III < II(b) II < III < I(c) III < II < I(d) I < II < III
›Reveal solutionSolution
SN1 reaction rate depends on the stability of the intermediate carbocation: tertiary > secondary > primary.
The SN1 mechanism proceeds via a carbocation intermediate formed by ionisation of the C–X bond in the rate-determining step. The MORE stable this carbocation, the FASTER the SN1 reaction — and carbocation stability increases with alkyl substitution (more +I donation and hyperconjugation stabilise the positive charge): 3° > 2° > 1°.
- (II) 1-Bromopentane — a primary halide, forms a primary carbocation (least stable) → SLOWEST SN1. …
- GUJCET 2024Set 131 markMCQQ.Predict the order of reactivity of the following compounds in SN1 reaction.(i) C6H5⋅CH2Br(ii) C6H5⋅CH⋅(C6H5)Br(iii) C6H5⋅CH(CH3)Br(iv) C6H5⋅C⋅(CH3)(C6H5)Br (A)(ii) >(iii) >(iv) >(i) (B)(ii) >(iv) >(iii) >(i) (C)(iv) >(iii) >(ii) >(i) (D)(iv) >(ii) >(iii) > (i)
›Reveal solutionSolution
More stabilising groups on the cationic carbon → faster SN1. Two phenyls beat one phenyl + methyl.
Concept. SN1 rate depends on the stability of the carbocation formed. Phenyl groups stabilise through resonance more strongly than a methyl stabilises by induction/hyperconjugation.
- (iv) C6H5C+(CH3)(C6H5): two phenyl + methyl — most stable.
- (ii) C6H5C+H(C6H5): two phenyl (benzhydryl). …
- GSEB Higher Secondary Certificate (HSC) Examination 2024Set ANNUAL1 markMCQQ.Predict the order of reactivity of the following compounds in SN1 reaction:(i) CH3CH2CH(Br)CH3(ii) (CH3)2CHCH2Br(iii) (CH3)3CBr(a)(iii) <(ii) <(i)(b)(ii) <(i) <(iii)(c)(i) <(ii) <(iii)(d)(iii) <(i) < (ii)
›Reveal solutionSolution
SN1 reaction rate depends on the stability of the carbocation intermediate formed; more substituted (more alkyl-stabilised) carbocations react faster via SN1.
- CH3CH2CH(Br)CH3 - a secondary alkyl halide (sec-butyl bromide), gives a secondary carbocation.
- (CH3)2CHCH2Br - a primary alkyl halide (isobutyl bromide), gives a primary carbocation (least stable).
- (CH3)3CBr - a tertiary alkyl halide (tert-butyl bromide), gives a tertiary carbocation (most stable, fastest SN1). …
- GUJCET 2021Set 151 markMCQQ.Which would undergo SN1 reaction faster from following? (A) Chloromethane (B) 2-bromo-3-methylbutane (C) 2-chloro-3-methylbutane (D) 2-bromo-2-methylpropane
›Reveal solutionSolution
SN1 rate tracks carbocation stability: tertiary + good leaving group = fastest.
Concept: SN1 is rate-determined by ionisation to a carbocation. Order of stability 3° > 2° > 1° > methyl; and C−Br ionises more easily than C−Cl (weaker bond, better leaving group).
- (A) Chloromethane → methyl cation (impossible) — slowest.
- (B) 2-bromo-3-methylbutane → 2° cation. …
- GSEB Higher Secondary Certificate (HSC) Examination 2020Set ANNUAL1 markMCQQ.Which of the following compound has highest reactivity towards SN1 reaction?(a) C6H5CH(C6H5)Br(b) C6H5CH2Br(c) C6H5C(CH3)(C6H5)Br(d) C6H5CH(CH3)Br
›Reveal solutionSolution
SN1 reactivity tracks carbocation stability: the more substituted and the more resonance-stabilised (benzylic) the resulting cation, the faster the SN1 reaction.
Ranking the carbocations that would form on loss of Br-:
- (b) C6H5CH2+ - primary benzylic cation, stabilised by only one phenyl ring.
- (d) C6H5CH(CH3)+ - secondary benzylic cation, one phenyl + one methyl.
- (a) C6H5CH(C6H5)+ - secondary but doubly-benzylic (two phenyl rings delocalise the charge) - more stable than (d). …
- GSEB Higher Secondary Certificate (HSC) Examination 2019Set ANNUAL1 markMCQQ.Which compound will give unimolecular nucleophilic substitution reaction easily with aqueous NaOH?(a) C6H5-CH2-CH2-Cl(b) C6H5-CH(Cl)-CH3(c) C6H5-C(Cl)(C6H5)-CH3(d) C6H5-CH2-Cl
›Reveal solutionSolution
SN1 reactions proceed through a carbocation intermediate, so the rate is fastest when the substrate can form the MOST STABLE carbocation -- tertiary and/or benzylic (resonance-stabilised) cations react fastest.
Comparing the stability of the carbocation each substrate would form on loss of Cl-:
- C6H5-CH2-CH2-Cl: ionisation gives a primary carbocation (not benzylic, since the CH2-Cl carbon is not directly attached to the ring) -- very unstable, SN1 disfavoured, reacts by SN2.
- C6H5-CH(Cl)-CH3: ionisation gives a SECONDARY benzylic carbocation (one phenyl ring for resonance stabilisation) -- reasonably stable, moderate SN1 reactivity. …
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