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Organic Chemistry and the New MCAT
Last updated: July 7th, 2023 |
Organic Chemistry and the MCAT,Ìýby Leah Fisch
Note from James: This is a guest post by Leah Fisch of , an online resource for learning organic chemistry, MCAT preparation, and other science topicsÌý.ÌýThis is a comprehensiveÌýLeah wrote on organic chemistry and the MCAT. You might want to bookmark this page for futureÌýreference, and be sure to visit Leah’s for more videos on nomenclature as well as other organic chemistry topics. Leah also tutors MCAT and organic chemistry. Ìý
Finally: If you’re planning on taking the MCAT soon, you should download Leah’s free .
Exactly how much organic chemistry is on the MCAT?
As a premed student, organic chemistry is likely one of the most difficult sciences you’ve encountered. Why take such a difficult course? Because you need it for the MCAT!
However, in 2015, when the MCAT exam changed, the amount of organic chemistry appeared to decrease, making students wonder just how much time they should dedicate to the topic.
Implication:Ìý“is it even worth it?”
The answer is tricky. So instead of telling you how much to study… let’s break it down.
The MCAT has a total of 4 sections covering 8 disciplines:
- Physics
- General Chemistry
- Organic Chemistry
- Biochemistry
- Biology
- Psychology
- Sociology
- Verbal Reasoning (CARS)
Organic chemistry is just ONE of the eight subjects you have to study.
But it gets better: Ìýorgo shows up in just the first and third section of the 7.5 hour exam.
Section 1: Chemical and Physical Foundations of Biological Systems is just 15% organic chemistry with the other 85% comprised of general chemistry, biochemistry, physics and biology.
Section 3: Biological and Biochemical Foundations of Living Systems is just 5% organic chemistry with the other 95% comprised of general chemistry, biochemistry and biology.
After a quick calculation organic chemistry appears to be just 5% of the entire exam!
But… don’t let the 5% estimate give you a false sense of security.
Biology is the most highly tested topic, but when you run the math it makes up just 18.75% of the MCAT.
Sounds low?
The math is somewhat misleading.
First of all, when medical schools evaluate your application, they look at more than just your total score. They look to see how you scored in each section, making organic chemistry suddenly more valuable. Consequently, even though it’s a small part of just two sections on the MCAT, skipping orgo study will tank your score in these sections, making you look bad.
The most important thing to recognize is just HOW organic chemistry is tested.
Fifteen percent of the first section doesn’t mean that 8.85 of 59 questions will be isolated organic chemistry questions.
Instead, the new MCAT is an integrated exam where you’ll be faced with research- and experiment-style passages combining multiple disciplines into a single passage and question:Ìý
- While you may not be asked for an R/S question directly, you may be asked about the optical purity of a newly synthesized experimental drug.
- You may not be tested on aldol condensations directly, but you may face a question asking you how glycolysis will be impacted by a single amino acid mutation in the active site of aldolase, which is the enzyme that catalyzes an aldol-style reaction in glycolysis.
Understanding Concepts is MUCH MORE Important than Memorization!Ìý
Your orgo professor likely asked FOR reactions, mechanisms, products, and lots of pushing arrows.
The MCAT is all multiple choice questions and applied concepts.
As you review reactions, don’t worry about memorizing mechanisms.
Instead, make sure to ask yourself these questions every step of the way.
- What is the purpose of this reaction?
- What is the purpose of this mechanism?
- What do I absolutely have to recognize about the reactant and reagent to help me understand the product? Focus on getting the logic, understanding the patterns and understanding what’s going on.
For example, Grignards are VERY reactive. They’ll attack all sorts of carbonyls. Don’t worry about which specific pair of electrons attack. Instead make sure you recognize the resulting alcohol product.
Why can’t you dissolve a Grignard in water or ethanol? Why should you complete the reaction with an acid workup AFTER the Grignard reacted? What happens if you mix the aqueous acid with the Grignard at the start of the reaction?
And most importantly, can you recognize the specific functional groups of this reaction when presented in the context of a biological or chemical research experiment?
As an MCAT tutor I’ve been interviewing students after each exam to understand the true nature of questions that arise on the exam.
This is where it gets interesting.
Once again, looking at just 15% orgo on the first section I notice an AVERAGE of 15% orgo questions. That is an average over the course of many exams combined.
One exam may have just two to three orgo questions about functional groups, SN1 reactions or IR spec, while another exam will have as many as 15 organic chemistry questions.
Another thing I’ve noticed is that while you may have learned a certain topic in your organic chemistry course, the MCAT will find a way to test it under the disguise of biology or biochemistry. This is especially true with , separation techniques and of course chirality.
This makes the value of your organic chemistry study much more significant, as orgo success will be success in the other subjects as well.
What does this mean for you as a premed student?
“What about high yield topics?”
Students looking for shortcuts often want to know which high-yield orgo topics to study.
In other words: “if I just have time to cover a bit of orgo, which topics should I focus on?”
This is a trick question.
I’ve heard from MCAT testers that any given MCAT has covered multiple passages on a single “low-yieldâ€� topic. Students who’ve studied everything will get these correct. Students who followed their MCAT book’s advice on high-yield topics ONLY wound up missing out on quite a few simple (low yield) questions.
For example, one of the 2016 MCATs had no less than FIVE passages related to lab separation techniques. If you thought, “sure I’ll cover electrophoresis quicklyâ€� and didn’t study it well enough, you would have missed out on several questions.
With all of this in mind, make sure you absolutely master the following starting with all of the beginner orgo topics typically covered in first semester organic chemistry. Then focus on understanding the patterns and functional groups of reactions covered in orgo 2.
Why? Because organic chemistry 2 is simply orgo 1 on steroids building on these very foundations.
Here’s my recommendation for what to cover when studying organic chemistry for the MCAT
The following is not an exhaustive list but a very good start on what to focus on:
1. Start With The Basics
The AAMC considers some of these “general chemistry� topics but you likely covered this in organic chemistry 1.
- Lewis structure and bonding
- Hybridization, bond angles and electronic/molecular geometry []
- Structural formulas including skeletal structure (bond line notation) []
Let’s face it, while you won’t be tested the nomenclature itself, you better know exactly what is meant by isopropyl, tert-butyl and more.
2. Isomers and Stereochemistry
- structural isomers (constitutional isomers) []
- conformational isomers including Newman and Chair
- Chirality including R/S, D/L, , meso compounds and more
- cis/trans and E/Z
- Acids & Bases: The non-math (non gen chem) aspect (such as acidity trends)
- SN1/SN2/E1/E2 188bet½ð±¦²©¹ÙÍøµÇ¼ and how to differentiate between them
3. The following topics are sometimes covered in Org 1 or Org 2. Learn these well but don’t go too crazy!
- Alcohols & Phenols: 188bet½ð±¦²©¹ÙÍøµÇ¼, protecting groups, leaving groups
- Aromaticity: Concept more than reactions including heterocyclic aromatic compounds
- Aldehyde and Ketone: Direct 188bet½ð±¦²©¹ÙÍøµÇ¼, (enolates), Keto-Enol Tautomerism (KET) and more
- Amine reactions especially as they relate to
- Carboxylic Acids: Formation and 188bet½ð±¦²©¹ÙÍøµÇ¼
- Carboxylic Acid Derivatives, especially esters in biological molecules
4. The following topics are often introduced in orgo but covered in biochemistry
- : orgo focus on Fischer Projections, stereochemistry and some reactions
- : orgo focus on Fischer Projections, stereochemistry and some reactions
5. And let’s not forget Lab Techniques
If the MCAT is all about experiments and research, make sure you know and truly understand the following analytical methods including simple graph interpretation:
- 13C and 1H-NMR []
- IR (Infrared spectroscopy)
- UV (Ultraviolet spectroscopy)
Separation Techniques
- Extraction
- Distillation
- Chromatography
6. What about all those crazy orgo 2 reactions not listed above?
Don’t skip them completely just in case.
Don’t go nuts as you review but simply look at your book and try to understand what’s going on.
For example Acetoacetic Ester Synthesis, Michael Addition and more. These are SPECIFIC reactions that incorporate bits and pieces of the reactions listed above.
So while you’re not required to know this mechanism, acetoacetic ester synthesis is really just a combination of the following reactions:
- Acid base
- SN2
- dehydration/elimination
- Keto Enol Tautomerization
I challenge you to go study the steps and verify that the above is true.Ìý
The MCAT EXPECTS you to recognize that this is the case, but in reality most students are under too much pressure to make these connections.
To be safe, spend some time each day watching a short advanced reaction mechanism tutorial video or reviewing a single reaction in your orgo book. Let the book/tutorial make the connections for you so that your brain power is reserved for figuring out what the heck they are asking in the passage/question.
Let’s take this to the extreme.
Nowhere on the AAMC outline do you see the mention of alkenes.
Does this mean you can skip it?ÌýNot quite!
Let’s read between the lines:
- E1/E2 including alcohol dehydration = alkenes.
- What if you reverse the reaction?ÌýThat’s an alkene addition reaction!
- What if you have to synthesize an alcohol?ÌýAlkenes make good starting points.
- What about Cis/Trans E/Z isomers as the product of a reaction?
Once again, alkene reactions.
And yes, MCAT testers HAVE confirmed seeing all of this on their MCAT.
What does this mean for you as a premed student?
Do NOT discount organic chemistry just because there’s so much else to study.
Instead I recommend breaking up your study schedule so that you devote time to cover a little bit of EACH MCAT topic on a weekly basis including organic chemistry.
So how do you structure your schedule in a manner that allows you to cover ALL of the content for the MCAT and work in practice questions and full lengths, without forgetting or burning out?
Thanks for demystifying the recent changes to the MCAT Leah – and best wishes to everyone for a successful test! – JÌý
00 General Chemistry Review
01 Bonding, Structure, and Resonance
- How Do We Know Methane (CH4) Is Tetrahedral?
- Hybrid Orbitals and Hybridization
- How To Determine Hybridization: A Shortcut
- Orbital Hybridization And Bond Strengths
- Sigma bonds come in six varieties: Pi bonds come in one
- A Key Skill: How to Calculate Formal Charge
- The Four Intermolecular Forces and How They Affect Boiling Points
- 3 Trends That Affect Boiling Points
- How To Use Electronegativity To Determine Electron Density (and why NOT to trust formal charge)
- Introduction to Resonance
- How To Use Curved Arrows To Interchange Resonance Forms
- Evaluating Resonance Forms (1) - The Rule of Least Charges
- How To Find The Best Resonance Structure By Applying Electronegativity
- Evaluating Resonance Structures With Negative Charges
- Evaluating Resonance Structures With Positive Charge
- Exploring Resonance: Pi-Donation
- Exploring Resonance: Pi-acceptors
- In Summary: Evaluating Resonance Structures
- Drawing Resonance Structures: 3 Common Mistakes To Avoid
- How to apply electronegativity and resonance to understand reactivity
- Bond Hybridization Practice
- Structure and Bonding Practice Quizzes
- Resonance Structures Practice
02 Acid Base 188bet½ð±¦²©¹ÙÍøµÇ¼
- Introduction to Acid-Base 188bet½ð±¦²©¹ÙÍøµÇ¼
- Acid Base 188bet½ð±¦²©¹ÙÍøµÇ¼ In Organic Chemistry
- The Stronger The Acid, The Weaker The Conjugate Base
- Walkthrough of Acid-Base 188bet½ð±¦²©¹ÙÍøµÇ¼ (3) - Acidity Trends
- Five Key Factors That Influence Acidity
- Acid-Base 188bet½ð±¦²©¹ÙÍøµÇ¼: Introducing Ka and pKa
- How to Use a pKa Table
- The pKa Table Is Your Friend
- A Handy Rule of Thumb for Acid-Base 188bet½ð±¦²©¹ÙÍøµÇ¼
- Acid Base 188bet½ð±¦²©¹ÙÍøµÇ¼ Are Fast
- pKa Values Span 60 Orders Of Magnitude
- How Protonation and Deprotonation Affect Reactivity
- Acid Base Practice Problems
03 Alkanes and Nomenclature
- Meet the (Most Important) Functional Groups
- Condensed Formulas: Deciphering What the Brackets Mean
- Hidden Hydrogens, Hidden Lone Pairs, Hidden Counterions
- Don't Be Futyl, Learn The Butyls
- Primary, Secondary, Tertiary, Quaternary In Organic Chemistry
- Branching, and Its Affect On Melting and Boiling Points
- The Many, Many Ways of Drawing Butane
- Wedge And Dash Convention For Tetrahedral Carbon
- Common Mistakes in Organic Chemistry: Pentavalent Carbon
- Table of Functional Group Priorities for Nomenclature
- Summary Sheet - Alkane Nomenclature
- Organic Chemistry IUPAC Nomenclature Demystified With A Simple Puzzle Piece Approach
- Boiling Point Quizzes
- Organic Chemistry Nomenclature Quizzes
04 Conformations and Cycloalkanes
- Staggered vs Eclipsed Conformations of Ethane
- Conformational Isomers of Propane
- Newman Projection of Butane (and Gauche Conformation)
- Introduction to Cycloalkanes
- Geometric Isomers In Small Rings: Cis And Trans Cycloalkanes
- Calculation of Ring Strain In Cycloalkanes
- Cycloalkanes - Ring Strain In Cyclopropane And Cyclobutane
- Cyclohexane Conformations
- Cyclohexane Chair Conformation: An Aerial Tour
- How To Draw The Cyclohexane Chair Conformation
- The Cyclohexane Chair Flip
- The Cyclohexane Chair Flip - Energy Diagram
- Substituted Cyclohexanes - Axial vs Equatorial
- Ranking The Bulkiness Of Substituents On Cyclohexanes: "A-Values"
- Cyclohexane Chair Conformation Stability: Which One Is Lower Energy?
- Fused Rings - Cis-Decalin and Trans-Decalin
- Naming Bicyclic Compounds - Fused, Bridged, and Spiro
- Bredt's Rule (And Summary of Cycloalkanes)
- Newman Projection Practice
- Cycloalkanes Practice Problems
05 A Primer On Organic 188bet½ð±¦²©¹ÙÍøµÇ¼
- The Most Important Question To Ask When Learning a New Reaction
- Curved Arrows (for reactions)
- Nucleophiles and Electrophiles
- The Three Classes of Nucleophiles
- Nucleophilicity vs. Basicity
- What Makes A Good Nucleophile?
- What Makes A Good Leaving Group?
- 3 Factors That Stabilize Carbocations
- Equilibrium and Energy Relationships
- 7 Factors that stabilize negative charge in organic chemistry
- 7 Factors That Stabilize Positive Charge in Organic Chemistry
- What's a Transition State?
- Hammond's Postulate
- Learning Organic Chemistry 188bet½ð±¦²©¹ÙÍøµÇ¼: A Checklist (PDF)
- Introduction to Oxidative Cleavage 188bet½ð±¦²©¹ÙÍøµÇ¼
06 Free Radical 188bet½ð±¦²©¹ÙÍøµÇ¼
- Bond Dissociation Energies = Homolytic Cleavage
- Free Radical 188bet½ð±¦²©¹ÙÍøµÇ¼
- 3 Factors That Stabilize Free Radicals
- What Factors Destabilize Free Radicals?
- Bond Strengths And Radical Stability
- Free Radical Initiation: Why Is "Light" Or "Heat" Required?
- Initiation, Propagation, Termination
- Monochlorination Products Of Propane, Pentane, And Other Alkanes
- Selectivity In Free Radical 188bet½ð±¦²©¹ÙÍøµÇ¼
- Selectivity in Free Radical 188bet½ð±¦²©¹ÙÍøµÇ¼: Bromination vs. Chlorination
- Halogenation At Tiffany's
- Allylic Bromination
- Bonus Topic: Allylic Rearrangements
- In Summary: Free Radicals
- Synthesis (2) - 188bet½ð±¦²©¹ÙÍøµÇ¼ of Alkanes
- Free Radicals Practice Quizzes
07 Stereochemistry and Chirality
- Types of Isomers: Constitutional Isomers, Stereoisomers, Enantiomers, and Diastereomers
- How To Draw The Enantiomer Of A Chiral Molecule
- How To Draw A Bond Rotation
- Introduction to Assigning (R) and (S): The Cahn-Ingold-Prelog Rules
- Assigning Cahn-Ingold-Prelog (CIP) Priorities (2) - The Method of Dots
- Enantiomers vs Diastereomers vs The Same? Two Methods For Solving Problems
- Assigning R/S To Newman Projections (And Converting Newman To Line Diagrams)
- How To Determine R and S Configurations On A Fischer Projection
- The Meso Trap
- Optical Rotation, Optical Activity, and Specific Rotation
- Optical Purity and Enantiomeric Excess
- What's a Racemic Mixture?
- Chiral Allenes And Chiral Axes
- Stereochemistry Practice Problems and Quizzes
08 Substitution 188bet½ð±¦²©¹ÙÍøµÇ¼
- Nucleophilic Substitution 188bet½ð±¦²©¹ÙÍøµÇ¼ - Introduction
- Two Types of Nucleophilic Substitution 188bet½ð±¦²©¹ÙÍøµÇ¼
- The SN2 Mechanism
- Why the SN2 Reaction Is Powerful
- The SN1 Mechanism
- The Conjugate Acid Is A Better Leaving Group
- Comparing the SN1 and SN2 188bet½ð±¦²©¹ÙÍøµÇ¼
- Polar Protic? Polar Aprotic? Nonpolar? All About Solvents
- Steric Hindrance is Like a Fat Goalie
- Common Blind Spot: Intramolecular 188bet½ð±¦²©¹ÙÍøµÇ¼
- Substitution Practice - SN1
- Substitution Practice - SN2
09 Elimination 188bet½ð±¦²©¹ÙÍøµÇ¼
- Elimination 188bet½ð±¦²©¹ÙÍøµÇ¼ (1): Introduction And The Key Pattern
- Elimination 188bet½ð±¦²©¹ÙÍøµÇ¼ (2): The Zaitsev Rule
- Elimination 188bet½ð±¦²©¹ÙÍøµÇ¼ Are Favored By Heat
- Two Elimination Reaction Patterns
- The E1 Reaction
- The E2 Mechanism
- E1 vs E2: Comparing the E1 and E2 188bet½ð±¦²©¹ÙÍøµÇ¼
- Antiperiplanar Relationships: The E2 Reaction and Cyclohexane Rings
- Bulky Bases in Elimination 188bet½ð±¦²©¹ÙÍøµÇ¼
- Comparing the E1 vs SN1 188bet½ð±¦²©¹ÙÍøµÇ¼
- Elimination (E1) 188bet½ð±¦²©¹ÙÍøµÇ¼ With Rearrangements
- E1cB - Elimination (Unimolecular) Conjugate Base
- Elimination (E1) Practice Problems And Solutions
- Elimination (E2) Practice Problems and Solutions
10 Rearrangements
11 SN1/SN2/E1/E2 Decision
- Identifying Where Substitution and Elimination 188bet½ð±¦²©¹ÙÍøµÇ¼ Happen
- Deciding SN1/SN2/E1/E2 (1) - The Substrate
- Deciding SN1/SN2/E1/E2 (2) - The Nucleophile/Base
- SN1 vs E1 and SN2 vs E2 : The Temperature
- Deciding SN1/SN2/E1/E2 - The Solvent
- Wrapup: The Key Factors For Determining SN1/SN2/E1/E2
- Alkyl Halide Reaction Map And Summary
- SN1 SN2 E1 E2 Practice Problems
12 Alkene 188bet½ð±¦²©¹ÙÍøµÇ¼
- E and Z Notation For Alkenes (+ Cis/Trans)
- Alkene Stability
- Alkene Addition 188bet½ð±¦²©¹ÙÍøµÇ¼: "Regioselectivity" and "Stereoselectivity" (Syn/Anti)
- Stereoselective and Stereospecific 188bet½ð±¦²©¹ÙÍøµÇ¼
- Hydrohalogenation of Alkenes and Markovnikov's Rule
- Hydration of Alkenes With Aqueous Acid
- Rearrangements in Alkene Addition 188bet½ð±¦²©¹ÙÍøµÇ¼
- Halogenation of Alkenes and Halohydrin Formation
- Oxymercuration Demercuration of Alkenes
- Hydroboration Oxidation of Alkenes
- m-CPBA (meta-chloroperoxybenzoic acid)
- OsO4 (Osmium Tetroxide) for Dihydroxylation of Alkenes
- Palladium on Carbon (Pd/C) for Catalytic Hydrogenation of Alkenes
- Cyclopropanation of Alkenes
- A Fourth Alkene Addition Pattern - Free Radical Addition
- Alkene 188bet½ð±¦²©¹ÙÍøµÇ¼: Ozonolysis
- Summary: Three Key Families Of Alkene Reaction Mechanisms
- Synthesis (4) - Alkene Reaction Map, Including Alkyl Halide 188bet½ð±¦²©¹ÙÍøµÇ¼
- Alkene 188bet½ð±¦²©¹ÙÍøµÇ¼ Practice Problems
13 Alkyne 188bet½ð±¦²©¹ÙÍøµÇ¼
- Acetylides from Alkynes, And Substitution 188bet½ð±¦²©¹ÙÍøµÇ¼ of Acetylides
- Partial Reduction of Alkynes With Lindlar's Catalyst
- Partial Reduction of Alkynes With Na/NH3 To Obtain Trans Alkenes
- Alkyne Hydroboration With "R2BH"
- Hydration and Oxymercuration of Alkynes
- Hydrohalogenation of Alkynes
- Alkyne Halogenation: Bromination, Chlorination, and Iodination of Alkynes
- Alkyne 188bet½ð±¦²©¹ÙÍøµÇ¼ - The "Concerted" Pathway
- Alkenes To Alkynes Via Halogenation And Elimination 188bet½ð±¦²©¹ÙÍøµÇ¼
- Alkynes Are A Blank Canvas
- Synthesis (5) - 188bet½ð±¦²©¹ÙÍøµÇ¼ of Alkynes
- Alkyne 188bet½ð±¦²©¹ÙÍøµÇ¼ Practice Problems With Answers
14 Alcohols, Epoxides and Ethers
- Alcohols - Nomenclature and Properties
- Alcohols Can Act As Acids Or Bases (And Why It Matters)
- Alcohols - Acidity and Basicity
- The Williamson Ether Synthesis
- Ethers From Alkenes, Tertiary Alkyl Halides and Alkoxymercuration
- Alcohols To Ethers via Acid Catalysis
- Cleavage Of Ethers With Acid
- Epoxides - The Outlier Of The Ether Family
- Opening of Epoxides With Acid
- Epoxide Ring Opening With Base
- Making Alkyl Halides From Alcohols
- Tosylates And Mesylates
- PBr3 and SOCl2
- Elimination 188bet½ð±¦²©¹ÙÍøµÇ¼ of Alcohols
- Elimination of Alcohols To Alkenes With POCl3
- Alcohol Oxidation: "Strong" and "Weak" Oxidants
- Demystifying The Mechanisms of Alcohol Oxidations
- Protecting Groups For Alcohols
- Thiols And Thioethers
- Calculating the oxidation state of a carbon
- Oxidation and Reduction in Organic Chemistry
- Oxidation Ladders
- SOCl2 Mechanism For Alcohols To Alkyl Halides: SN2 versus SNi
- Alcohol 188bet½ð±¦²©¹ÙÍøµÇ¼ Roadmap (PDF)
- Alcohol Reaction Practice Problems
- Epoxide Reaction Quizzes
- Oxidation and Reduction Practice Quizzes
15 Organometallics
- What's An Organometallic?
- Formation of Grignard and Organolithium Reagents
- Organometallics Are Strong Bases
- 188bet½ð±¦²©¹ÙÍøµÇ¼ of Grignard Reagents
- Protecting Groups In Grignard 188bet½ð±¦²©¹ÙÍøµÇ¼
- Synthesis Problems Involving Grignard Reagents
- Grignard 188bet½ð±¦²©¹ÙÍøµÇ¼ And Synthesis (2)
- Organocuprates (Gilman Reagents): How They're Made
- Gilman Reagents (Organocuprates): What They're Used For
- The Heck, Suzuki, and Olefin Metathesis 188bet½ð±¦²©¹ÙÍøµÇ¼ (And Why They Don't Belong In Most Introductory Organic Chemistry Courses)
- Reaction Map: 188bet½ð±¦²©¹ÙÍøµÇ¼ of Organometallics
- Grignard Practice Problems
16 Spectroscopy
- Degrees of Unsaturation (or IHD, Index of Hydrogen Deficiency)
- Conjugation And Color (+ How Bleach Works)
- Introduction To UV-Vis Spectroscopy
- UV-Vis Spectroscopy: Absorbance of Carbonyls
- UV-Vis Spectroscopy: Practice Questions
- Bond Vibrations, Infrared Spectroscopy, and the "Ball and Spring" Model
- Infrared Spectroscopy: A Quick Primer On Interpreting Spectra
- IR Spectroscopy: 4 Practice Problems
- 1H NMR: How Many Signals?
- Homotopic, Enantiotopic, Diastereotopic
- Diastereotopic Protons in 1H NMR Spectroscopy: Examples
- 13-C NMR - How Many Signals
- Liquid Gold: Pheromones In Doe Urine
- Natural Product Isolation (1) - Extraction
- Natural Product Isolation (2) - Purification Techniques, An Overview
- Structure Determination Case Study: Deer Tarsal Gland Pheromone
17 Dienes and MO Theory
- What To Expect In Organic Chemistry 2
- Are these molecules conjugated?
- Conjugation And Resonance In Organic Chemistry
- Bonding And Antibonding Pi Orbitals
- Molecular Orbitals of The Allyl Cation, Allyl Radical, and Allyl Anion
- Pi Molecular Orbitals of Butadiene
- 188bet½ð±¦²©¹ÙÍøµÇ¼ of Dienes: 1,2 and 1,4 Addition
- Thermodynamic and Kinetic Products
- More On 1,2 and 1,4 Additions To Dienes
- s-cis and s-trans
- The Diels-Alder Reaction
- Cyclic Dienes and Dienophiles in the Diels-Alder Reaction
- Stereochemistry of the Diels-Alder Reaction
- Exo vs Endo Products In The Diels Alder: How To Tell Them Apart
- HOMO and LUMO In the Diels Alder Reaction
- Why Are Endo vs Exo Products Favored in the Diels-Alder Reaction?
- Diels-Alder Reaction: Kinetic and Thermodynamic Control
- The Retro Diels-Alder Reaction
- The Intramolecular Diels Alder Reaction
- Regiochemistry In The Diels-Alder Reaction
- The Cope and Claisen Rearrangements
- Electrocyclic 188bet½ð±¦²©¹ÙÍøµÇ¼
- Electrocyclic Ring Opening And Closure (2) - Six (or Eight) Pi Electrons
- Diels Alder Practice Problems
- Molecular Orbital Theory Practice
18 Aromaticity
- Introduction To Aromaticity
- Rules For Aromaticity
- Huckel's Rule: What Does 4n+2 Mean?
- Aromatic, Non-Aromatic, or Antiaromatic? Some Practice Problems
- Antiaromatic Compounds and Antiaromaticity
- The Pi Molecular Orbitals of Benzene
- The Pi Molecular Orbitals of Cyclobutadiene
- Frost Circles
- Aromaticity Practice Quizzes
19 188bet½ð±¦²©¹ÙÍøµÇ¼ of Aromatic Molecules
- Electrophilic Aromatic Substitution: Introduction
- Activating and Deactivating Groups In Electrophilic Aromatic Substitution
- Electrophilic Aromatic Substitution - The Mechanism
- Ortho-, Para- and Meta- Directors in Electrophilic Aromatic Substitution
- Understanding Ortho, Para, and Meta Directors
- Why are halogens ortho- para- directors?
- Disubstituted Benzenes: The Strongest Electron-Donor "Wins"
- Electrophilic Aromatic Substitutions (1) - Halogenation of Benzene
- Electrophilic Aromatic Substitutions (2) - Nitration and Sulfonation
- EAS 188bet½ð±¦²©¹ÙÍøµÇ¼ (3) - Friedel-Crafts Acylation and Friedel-Crafts Alkylation
- Intramolecular Friedel-Crafts 188bet½ð±¦²©¹ÙÍøµÇ¼
- Nucleophilic Aromatic Substitution (NAS)
- Nucleophilic Aromatic Substitution (2) - The Benzyne Mechanism
- 188bet½ð±¦²©¹ÙÍøµÇ¼ on the "Benzylic" Carbon: Bromination And Oxidation
- The Wolff-Kishner, Clemmensen, And Other Carbonyl Reductions
- More 188bet½ð±¦²©¹ÙÍøµÇ¼ on the Aromatic Sidechain: Reduction of Nitro Groups and the Baeyer Villiger
- Aromatic Synthesis (1) - "Order Of Operations"
- Synthesis of Benzene Derivatives (2) - Polarity Reversal
- Aromatic Synthesis (3) - Sulfonyl Blocking Groups
- Birch Reduction
- Synthesis (7): Reaction Map of Benzene and Related Aromatic Compounds
- Aromatic 188bet½ð±¦²©¹ÙÍøµÇ¼ and Synthesis Practice
- Electrophilic Aromatic Substitution Practice Problems
20 Aldehydes and Ketones
- What's The Alpha Carbon In Carbonyl Compounds?
- Nucleophilic Addition To Carbonyls
- Aldehydes and Ketones: 14 188bet½ð±¦²©¹ÙÍøµÇ¼ With The Same Mechanism
- Sodium Borohydride (NaBH4) Reduction of Aldehydes and Ketones
- Grignard Reagents For Addition To Aldehydes and Ketones
- Wittig Reaction
- Hydrates, Hemiacetals, and Acetals
- Imines - Properties, Formation, 188bet½ð±¦²©¹ÙÍøµÇ¼, and Mechanisms
- All About Enamines
- Breaking Down Carbonyl Reaction Mechanisms: 188bet½ð±¦²©¹ÙÍøµÇ¼ of Anionic Nucleophiles (PartÌý2)
- Aldehydes Ketones Reaction Practice
21 Carboxylic Acid Derivatives
- Nucleophilic Acyl Substitution (With Negatively Charged Nucleophiles)
- Addition-Elimination Mechanisms With Neutral Nucleophiles (Including Acid Catalysis)
- Basic Hydrolysis of Esters - Saponification
- Transesterification
- Proton Transfer
- Fischer Esterification - Carboxylic Acid to Ester Under Acidic Conditions
- Lithium Aluminum Hydride (LiAlH4) For Reduction of Carboxylic Acid Derivatives
- LiAlH[Ot-Bu]3 For The Reduction of Acid Halides To Aldehydes
- Di-isobutyl Aluminum Hydride (DIBAL) For The Partial Reduction of Esters and Nitriles
- Amide Hydrolysis
- Thionyl Chloride (SOCl2) And Conversion of Carboxylic Acids to Acid Halides
- Diazomethane (CH2N2)
- Carbonyl Chemistry: Learn Six Mechanisms For the Price Of One
- Making Music With Mechanisms (PADPED)
- Carboxylic Acid Derivatives Practice Questions
22 Enols and Enolates
- Keto-Enol Tautomerism
- Enolates - Formation, Stability, and Simple 188bet½ð±¦²©¹ÙÍøµÇ¼
- Kinetic Versus Thermodynamic Enolates
- Aldol Addition and Condensation 188bet½ð±¦²©¹ÙÍøµÇ¼
- 188bet½ð±¦²©¹ÙÍøµÇ¼ of Enols - Acid-Catalyzed Aldol, Halogenation, and Mannich 188bet½ð±¦²©¹ÙÍøµÇ¼
- Claisen Condensation and Dieckmann Condensation
- Decarboxylation
- The Malonic Ester and Acetoacetic Ester Synthesis
- The Michael Addition Reaction and Conjugate Addition
- The Robinson Annulation
- Haloform Reaction
- The Hell–Volhard–Zelinsky Reaction
- Enols and Enolates Practice Quizzes
23 Amines
- The Amide Functional Group: Properties, Synthesis, and Nomenclature
- Basicity of Amines And pKaH
- 5 Key Basicity Trends of Amines
- The Mesomeric Effect And Aromatic Amines
- Nucleophilicity of Amines
- Alkylation of Amines (Sucks!)
- Reductive Amination
- The Gabriel Synthesis
- Some 188bet½ð±¦²©¹ÙÍøµÇ¼ of Azides
- The Hofmann Elimination
- The Hofmann and Curtius Rearrangements
- The Cope Elimination
- Protecting Groups for Amines - Carbamates
- The Strecker Synthesis of Amino Acids
- Introduction to Peptide Synthesis
- 188bet½ð±¦²©¹ÙÍøµÇ¼ of Diazonium Salts: Sandmeyer and Related 188bet½ð±¦²©¹ÙÍøµÇ¼
- Amine Practice Questions
24 Carbohydrates
- D and L Notation For Sugars
- Pyranoses and Furanoses: Ring-Chain Tautomerism In Sugars
- What is Mutarotation?
- Reducing Sugars
- The Big Damn Post Of Carbohydrate-Related Chemistry Definitions
- The Haworth Projection
- Converting a Fischer Projection To A Haworth (And Vice Versa)
- 188bet½ð±¦²©¹ÙÍøµÇ¼ of Sugars: Glycosylation and Protection
- The Ruff Degradation and Kiliani-Fischer Synthesis
- Isoelectric Points of Amino Acids (and How To Calculate Them)
- Carbohydrates Practice
- Amino Acid Quizzes
25 Fun and Miscellaneous
- A Gallery of Some Interesting Molecules From Nature
- Screw Organic Chemistry, I'm Just Going To Write About Cats
- On Cats, Part 1: Conformations and Configurations
- On Cats, Part 2: Cat Line Diagrams
- On Cats, Part 4: Enantiocats
- On Cats, Part 6: Stereocenters
- Organic Chemistry Is Shit
- The Organic Chemistry Behind "The Pill"
- Maybe they should call them, "Formal Wins" ?
- Why Do Organic Chemists Use Kilocalories?
- The Principle of Least Effort
- Organic Chemistry GIFS - Resonance Forms
- Reproducibility In Organic Chemistry
- What Holds The Nucleus Together?
- How 188bet½ð±¦²©¹ÙÍøµÇ¼ Are Like Music
- Organic Chemistry and the New MCAT
26 Organic Chemistry Tips and Tricks
- Common Mistakes: Formal Charges Can Mislead
- Partial Charges Give Clues About Electron Flow
- Draw The Ugly Version First
- Organic Chemistry Study Tips: Learn the Trends
- The 8 Types of Arrows In Organic Chemistry, Explained
- Top 10 Skills To Master Before An Organic Chemistry 2 Final
- Common Mistakes with Carbonyls: Carboxylic Acids... Are Acids!
- Planning Organic Synthesis With "Reaction Maps"
- Alkene Addition Pattern #1: The "Carbocation Pathway"
- Alkene Addition Pattern #2: The "Three-Membered Ring" Pathway
- Alkene Addition Pattern #3: The "Concerted" Pathway
- Number Your Carbons!
- The 4 Major Classes of 188bet½ð±¦²©¹ÙÍøµÇ¼ in Org 1
- How (and why) electrons flow
- Grossman's Rule
- Three Exam Tips
- A 3-Step Method For Thinking Through Synthesis Problems
- Putting It Together
- Putting Diels-Alder Products in Perspective
- The Ups and Downs of Cyclohexanes
- The Most Annoying Exceptions in Org 1 (Part 1)
- The Most Annoying Exceptions in Org 1 (Part 2)
- The Marriage May Be Bad, But the Divorce Still Costs Money
- 9 Nomenclature Conventions To Know
- Nucleophile attacksÌýElectrophile
27 Case Studies of Successful O-Chem Students
- Success Stories: How Corina Got The The "Hard" Professor - And Got An A+ Anyway
- How Helena Aced Organic Chemistry
- From a "Drop" To B+ in Org 2 � How A Hard Working Student Turned It Around
- How Serge Aced Organic Chemistry
- Success Stories: How Zach Aced Organic Chemistry 1
- Success Stories: How Kari Went From C� to B+
- How Esther Bounced Back From a "C" To Get A's In Organic Chemistry 1 And 2
- How Tyrell Got The Highest Grade In Her Organic Chemistry Course
- This Is Why Students Use Flashcards
- Success Stories: How Stu Aced Organic Chemistry
- How John Pulled Up His Organic Chemistry Exam Grades
- Success Stories: How Nathan Aced Organic Chemistry (Without It Taking Over His Life)
- How Chris Aced Org 1 and Org 2
- Interview: How Jay Got an A+ In Organic Chemistry
- How to Do Well in Organic Chemistry: One Student's Advice
- "America's Top TA" Shares His Secrets For Teaching O-Chem
- "Organic Chemistry Is Like..." - A Few Metaphors
- How To Do Well In Organic Chemistry: Advice From A Tutor
- Guest post: "I went from being afraid of tests to actually looking forward to them".
Oh my gosh Leah!!! Her Youtube videos and your blog singlehandedly saved my organic chemistry grades. Feels like a legendary collab for that reason haha.
Thanks Leah! It refocused Orgo studying for me!
You’re very welcome Saima. Glad to help
I’m trying to get the hang of Orgo. I’ve had a few breakthroughs that I’m happy about. I never really learned about the carbonyl carbon’s partial positive charge in GC, but now I understand the reason why nucleophiles act the way they do.
Brandy: Every orgo course is different. Go into MCAT prep thinking ‘clean slate, do I get this?’ to ensure you cover everything AND understand what you study
Let’s not forget that you can’t really understand biochemistry without organic, ultimately making it a larger part of the mcat than most would think. Never neglect your orgo skills!
Too true @Joanna. Many students fear biochem especially if they haven’t taken it. But it’s really just gen chem + bio + orgo brought to life.
Great Info Leah! I definitely will not be underestimating my O-Chem studies. Thanks
You’re very welcome. Never underestimate your studies, especially the premed courses. You never know when you’ll need them again