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Organic Chemistry Exam Q&A (100+) | Reaction Mechanisms, Nucleophiles, Aromatics, Stereochemistry | 2025/2026 | Chemistry Department

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This document includes over 100 structured and solved exam questions covering key principles of Organic Chemistry, curated for the 2025/2026 academic year at [University Name]. It thoroughly reviews topics essential for foundational and intermediate-level organic chemistry students, focusing on both theoretical understanding and applied reaction logic. Key subject areas include: Reaction mechanisms: SN1, SN2, E1, and E2 processes, including reaction conditions, carbocation stability, and transition state analysis Nucleophiles and electrophiles: Comparative strength, influence of solvent, and reactivity in substitution/elimination contexts Stereochemistry: R/S configuration, optical activity, chirality, meso compounds, enantiomers, and diastereomers Aromaticity and aromatic substitution: Hückel’s rule, electrophilic aromatic substitution (EAS), activating/deactivating groups, and regioselectivity Hydrocarbons and functional groups: Alkanes, alkenes, alkynes, alcohols, ethers, ketones, and carboxylic acids Reagents and synthesis: Grignard reagents, PCC, KMnO₄, LAH, DIBAL, HBr/ROOR mechanisms Acid-base reactions: pKa values, resonance stabilization, inductive effects Spectroscopy-based ID (IR, NMR basics) and resonance structures Practice with curved arrow notation, intermediates, and product prediction under various lab conditions This resource is highly recommended for: Undergraduate chemistry and pre-medical students Learners preparing for organic chemistry midterms, finals, MCAT, or other standardized exams Students needing reaction mechanism practice and visual stepwise explanations Anyone revising for conceptual and applied organic synthesis questions The format encourages pattern recognition in reactivity, product prediction, and mechanism mapping—making it ideal for rapid study, problem-solving drills, or foundational review. Keywords: organic chemistry, SN1, SN2, E1, E2, nucleophile, electrophile, leaving group, substitution, elimination, stereochemistry, chirality, enantiomers, diastereomers, meso compound, aromaticity, Hückel’s rule, EAS, Grignard, PCC, KMnO₄, LAH, DIBAL, pKa, resonance, IR spectroscopy, NMR, reaction mechanism, curved arrow, acid-base, functional groups, product prediction, MCAT chemistry

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Organic Chemistry 1
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Organic Chemistry 1











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Institution
Organic Chemistry 1
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Uploaded on
December 14, 2025
Number of pages
121
Written in
2025/2026
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Exam (elaborations)
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Organic Chemistry (Kaplan MCAT)
2025/2026 Exam Questions with 100%
Correct Answers | Latest Update



Chapter 1 - 🧠ANSWER ✔✔CH1 Nomenclature


organic chemistry - 🧠ANSWER ✔✔the study of all chemicals containing

carbon


Arrhenius acid - 🧠ANSWER ✔✔Produces H+ ions when dissolved in water


*acids=selfish, they take (e-) and kick (H+)


Arrhenius base - 🧠ANSWER ✔✔Produces OH- ions when dissolved in

water

*bases=kind, they donate (e-) and shelter (H+)

,nomenclature naming cheatsheet - 🧠ANSWER ✔✔5 ways to look at name:


1. Prefix-longestchain-suffix

2. 2@carbonchain-suffix

3. #-substituent-base-boss

4. least reactive-chain-most reactive

5. ordering of C start from the end with the boss/most reactive group




ex. 2,2-ethyl-4methylhept-ene-ioc acid (most oxidizing at end)


nomenclature based on alkyl-substituent branching: - 🧠ANSWER ✔✔n-

=normal flat chain

t- =3 leaf clover shape

neo- =4 leaf clover shape

iso- =fork split at end

sec- =branch off on nonterminal C

tran- =branches opposite side (ex. geminal diol)

cis= =branches same side (ex. vicinal diol)

,cyclo- =in ring

10 Nomenclature (Name/shape/prefix/suffix/ex) cheatsheet: - 🧠ANSWER

✔✔In order of reactivity/priority...


1. Carboxylic acids (-COOH)=carboxy-/-oic acid/ ex. butanoic acid

2. Anhydride (O=C-O-C=O)=necklace shape/alkanoyloxycarbonyl-/-

anhydride/ ex. butyric anhydride

3. Ester (-COOR)=alkoxycarbonyl-/-oate/ex. ethyl butanoate

4. amide(-NH)= amido-/-amide/ex. butanamide

5. aldehyde (-O=CH)= oxo-/-al/ex. butanal

6. ketone (O=<CC)=carkey/oxo- or keto-/-one/ex. butanone

7. alcohol (-COH)= hydroxy-/-ol/ex. butanol

8. alkene (C=C)=alkenyl-/-ene/ex. butene

9. alkyne (C≡C)=alkynyl-/-yne/ex. butyne

10. alkane (C-C)=alkyl-/-ane/ex. butane




3
COPYRIGHT©JOSHCLAY 2025/2026. YEAR PUBLISHED 2025. COMPANY REGISTRATION NUMBER: 619652435. TERMS OF USE. PRIVACY
STATEMENT. ALL RIGHTS RESERVED

, *3 carboxylic acid derivatives=ester, amide, anhydrides


alkanes - 🧠ANSWER ✔✔a hydrocarbon containing only single covalent

bonds

Ex. CH4


Name alkanes with 1-12Cs - 🧠ANSWER ✔✔1=methane,


2=ethane,

3=propane,

4=butane,

5=pentane,

6=hexane,

7=heptane,

8=octane,

9=nonane,

10=decane,

11=undecane, (why it starting to sound spanish?)

12dodecane (oh right it's latin)

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