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JHUJohns Hopkins
MCATMCAT
ACSACS
AP CBAP College Board
AAMCAAMC
DATDAT/PCAT
TPRPrinceton Review
KPLNKaplan
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Chemistry.

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The Problem

This question is on your midterm. In 4 minutes.

68% of pre-med students fail Organic Chemistry I on their first attempt. Most knew the material — they just never saw it explained the right way.

CHEM 2320 · Midterm Exam II
Time Remaining240s

Question 14 of 40 · 2.5 pts

Which of the following correctly describes the mechanism of 
electrophilic aromatic substitution in the nitration of benzene?

A) The electrophile NO₂⁺ attacks the π system, forming an arenium ion intermediate, 
   followed by loss of H⁺ to restore aromaticity.

B) The reaction proceeds via an SN2 mechanism at the ring carbon, 
   with direct displacement of a hydrogen atom.

C) The nitro group replaces a carbon in the ring via a radical mechanism 
   initiated by UV light.

D) Benzene undergoes addition across a double bond, 
   forming a stable cyclohexane derivative.
AThe electrophile NO₂⁺ attacks the π system…
BSN2 mechanism at ring carbon…
CRadical mechanism via UV light…
DAddition across a double bond…
Most students guess here. There's a faster way to know.
Scroll to see it solved
The Catalyst Method

Same question. Now watch it collapse.

Step through each part of the mechanism. This is exactly how our lessons are structured — not memorization, but understanding.

Step 1 of 4

Step 1

Identify the Mechanism Type

EAS (Electrophilic Aromatic Substitution) is the key. Any time benzene reacts with a strong electrophile, this is your mechanism. The aromatic ring acts as the nucleophile.

Keyword: "Electrophilic" → EAS

Mechanism

Benzene + E⁺ → Arenium Ion → Product

Every lesson in Catalyst follows this exact structure. Visual → Mechanism → Why it matters.

Curriculum

Six modules. One semester in 30 hours.

Built around the exact topics that appear on MCAT, DAT, PCAT, and AP exams. Each node activates as you scroll — just like your understanding will.

01
MOD 01

Atomic Structure & Bonding

Foundation
Orbital theoryHybridizationVSEPRElectronegativity
02
MOD 02

Functional Groups & Nomenclature

Core
IUPAC namingAlkanes to aromaticsFunctional group IDIsomers
03
MOD 03

Reaction Mechanisms

High Yield
SN1 & SN2E1 & E2Addition reactionsEAS deep dive
04
MOD 04

Stereochemistry

MCAT Favorite
R/S configurationEnantiomersDiastereomersOptical activity
05
MOD 05

Carbonyl Chemistry

High Yield
Aldehydes & ketonesCarboxylic acidsNucleophilic acyl sub.Enolates
06
MOD 06

Exam Strategy & Timed Practice

Final Prep
Timed setsQuestion pattern recognitionElimination tacticsFull mock exams
Evidence

Built by chemists. Proven by outcomes.

Our instructors aren't influencers. They're researchers and former exam graders who built Catalyst because the existing tools weren't working.

Dr. Priya Venkataraman, PhD chemist with long dark hair in lab coat, smiling

97%

Student pass rate

Dr. Priya Venkataraman

Lead Organic Chemistry Instructor

  • PhD Chemistry, Stanford University
  • Former MCAT Prep Director, Kaplan
  • 12 years university teaching
  • 4,200+ students passed
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4.9

Average lesson rating

Marcus Osei, PhD(c)

General & AP Chemistry Specialist

  • PhD Candidate, Johns Hopkins
  • AP Chemistry Exam grader, 3 years
  • National Teaching Award 2023
  • 1,800+ AP students mentored

Student Outcome Data · Cohort 2023–2025 · n=12,400

92%

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vs. 41% national average

30 hrs

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