This interactive module is part of Founding Pro
You can still read this page for free. Upgrade to unlock full interaction and HD video downloads from the available catalog.
chemistry/curly-arrow
View PricingNucleophilic Substitution Mechanisms: Electron Pathfinder
Draw curly arrows to trace electron flow in nucleophilic substitution reactions. Master SN2 and SN1 mechanisms.
Upgrade to Founding Pro to unlock downloads
Key Concepts
Curly Arrows
Full arrows (⟶) show movement of electron pairs. They always start from an electron source (lone pair or bond).
Nucleophile & Electrophile
Nucleophiles donate electrons (electron-rich). Electrophiles accept electrons (electron-poor).
Leaving Groups
Good leaving groups (Br⁻, Cl⁻, I⁻) can stabilize negative charge and depart with the bonding electrons.
Understanding Nucleophilic Substitution Mechanisms
**Curly Arrows** are the graphical notation used by chemists to represent the movement of electron pairs during a reaction mechanism. They serve as the essential visual tool for predicting how bonds are broken and formed.
In organic chemistry, a full-headed curly arrow represents the movement of two electrons, always originating from an **electron source** (lone pair or bond) and pointing toward an **electron sink** (electrophilic center).
Use our interactive 'Electron Pathfinder' to draw step-by-step mechanisms for **SN1** and **SN2** reactions, receiving real-time validation for your nucleophilic attacks and leaving group departures.
Frequently Asked Questions
Related Simulations

Nucleophilic Substitution & β-Elimination
Interactive 3D visualization of nucleophilic substitution and β-elimination reactions of bromoethane.

Hydrocarbon Derivatives
**Hydrocarbon Derivatives** are organic compounds formed by replacing hydrogen atoms with specific **functional groups** containing oxygen, halogens, or nitrogen. This resource explores **Alcohols**, **Aldehydes**, **Carboxylic Acids**, and more.

Intermolecular Forces
**Intermolecular Forces (IMFs)** are the electrostatic attractions between neighboring molecules. This interactive lab compares the strength of **Hydrogen Bonding**, **Dipole-Dipole**, and **London Dispersion Forces**.