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Chemistry in a Nutshell
@ChemistryinaNutshellTracked since Jun 2026
Ph.D. Chemist | Passionate Educator | Science Enthusiast.
Observed Aug 26, 2026 · staleModeled revenue
Paid members
1
0% · 30-day rate from 23 observed days
Total audience
438
incl. free followers
Estimated monthly gross
$5
Starting price
$5/mo
2 membership tiers
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$0/moFreePublic prices and benefits only
$5/moBuy the Professor a TeaSupport Free Chemistry Education!🧪 Your $5 contribution is like buying me a cup of tea to keep the chemistry juices flowing during those late-night editing sessions. With enough support, I’ll be able to make more videos and continue to improve their quality. My current goal is to make a video for every topic covered in both general and organic chemistry. With enough support, I could make this a reality in 2 years instead of 10!You'll Receive:A Virtual "Cheers": My sincere gratitude for helping keep this educational resource free for students worldwide.Direct Impact: The knowledge that you are directly accelerating the timeline to turn this "Masterclass" into a complete library for gen chem and ochem.
Growth signals: Chemistry in a Nutshell
0%
Membership1 paid members · 30-day rate from 23 observed days
121
Jun 202613 weeks trackedNow
Chemistry in a Nutshell1 members · $5/mo
The chart only uses Chemistry in a Nutshell's observed public history. Comparison peers are listed below, but comparable trend series are not available yet.
Where Chemistry in a Nutshell ranks
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No comparable peer is available yet, so Chemistry in a Nutshell's cohort rank cannot be calculated.Ranking data · includes stale rows| Rank | Creator and why included | Paid members | Gap vs Chemistry in a Nutshell | Freshness |
|---|---|---|---|---|
| Not ranked |  Chemistry in a NutshellProfileUncategorizedPaid members position in Recommended cohort | 1 | Reference | Aug 26, 2026Stale |
The rank uses the full fixed cohort. This table shows up to five creators around Chemistry in a Nutshell; the coverage summary above still counts everyone.
Recent posts
What they publish61Profile posts4 postsLast month0%Members-only
Previews available for 25 of 61 posts
Article Latest postPublicOrganic Chemistry Reaction Mechanisms Survival Guide (Beta Release!)Hey everyone! I’m so excited to finally share the first version of the 60-page Organic Chemistry Reaction Mechanisms Survival Guide PDF.
August 30 0 likes 0 commentsFischer to Skeletal: The "Caterpillar" MethodAugust 10ArticleAugust 10Public 0 0How to Find Formal Charge from a Lewis StructureStop wasting time calculating formal charges. I’ll teach you my go-to shortcut that helps you find the formal charge on any atom in seconds, followed by 6 practice problems to make sure it sticks. It's as easy as counting the lines and dots in a Lewis Structure.AudioJuly 27Public 0 0Stop Guessing Hydrogens: Read Line Structures in 3 MinutesLine structures are the essential shorthand that every organic chemist needs to master. Whether you call them bond structures, bond line structures, or skeletal structures, the goals are the same: find the carbons, see the hidden hydrogens, and instantly understand what the drawings represent.AudioJuly 20Public 0 0Don't Start Ochem Until You Watch This (8 Essential Habits)July 13 View post Stop memorizing organic chemistry and start mastering its logic. Many straight-A students hit a wall in ochem because they try to study it like biology. Ochem isn't a subject to be memorized: It's a system to be dissected. Today, I'm breaking down the 8 essential habits that separate the top 1% of students from the rest of the class. 0:00 Why Do Straight-A Students Fail Chemistry? 0:19 Using Molecular Models for 3D Visualization 0:50 Ochem is a Sport: Why Practice Beats Reading 1:35 Less Memorizing; More Dissecting 2:35 How to Use Office Hours Effectively 3:23 Mastering Reaction Prediction 4:06 The Notecard MethodAudioJuly 13Public 0 0Why You Can NEVER Rotate this 90°June 15 View post Don't let the simplicity of this molecule fool you! Perspective structures are designed to be intuitive, but the Fischer Projection requires a specific "hugging" confirmation that most students forget when they're in a hurry. Today, we tackle the Rotation Trap: The #1 reason students get R/S configuration WRONG! If you’ve ever felt "3D Blind" when rotating a carbon backbone, this 2-minute masterclass is the cure. What You'll Learn: • The Hug Rule: Why the "Caterpillar" orientation is non-negotiable. • The Rotation Trap: How rotating a single bond can flip your R/S labels if you aren't careful. • Skeletal vs. Fischer: The final conversionArticleJune 15Public 0 0Converting D-Glucose: Skeletal Structure to Fischer Projection (5-Step System)Converting to a Fischer Projection on hard mode isn't about more rules: It's about more nuance. Today, we tackle the conversion of D-glucose from a skeletal structure to a Fischer projection. When molecules reach this size, physical models begin to fall apart due to steric hindrance. (The caterpillar literally bites its own tail.) I'll show you what to do when your model kit is lagging behind and how to rely on the 5-Step System to navigate multiple chiral centers without losing a single atom.ImageToday at Aug 26 crawlPublic 0 0The "Caterpillar" Secret to Fischer Projections (Never Miss a Carbon)Think you know Fischer projections? It's easy when there's only one chiral center, but everything changes when you have a 2,3-dibromobutane backbone. Learn the 4 step conversion process that works for any molecule, big or small! Today, we're dissecting the "zig-zag" skeletal to Fischer conversion, specifically focusing on the 2-center trap that causes 90% of stereochemistry errors on exams.ArticleToday at Aug 26 crawlPublic 0 0Newman to Perspective: Never Guess Your Wedges AgainMay 6ArticleMay 6Public 0 03 Traps That Kill Your Grade: Perspective to Newman ProjectionsMay 4ArticleMay 4Public 0 0The SN2 "Gotcha" That Most Students MissApril 6ArticleApril 6Public 0 06 Traps That Kill Your Grade: Converting Condensed to Skeletal StructuresMarch 26ArticleMarch 26Public 0 0
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