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Fundamental Concepts In Organic Reaction Mechanism
Chapter Name : Organic Chemistry - Some Basic Principles And Techniques
Sub Topic Code : 102_11_12_07_02
Topic Name : Fundamental Concepts In Organic Reaction Mechanism
Sub Topic Name : Nucleophiles And Electrophiles
Introduction

Organic chemistry is a chemistry sub discipline involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms.

Pre-Requisites:

Organic chemistry

Activity:

Aromatic compounds.

Real Life Question:

What is organic chemistry?

Key Words / FlashCards
Key Words Definitions (pref. in our own words)
nucleophile A nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in relation to a reaction.
Learning aids / Gadgets
Gadgets How it can be used
Alcohols Alcohols (R-OH) take the suffix "-ol" with an infix numerical bonding position: CH3CH2CH2OH is propan-1-ol. The suffixes -diol, -triol, -tetraol, etc., are used for multiple -OH groups: Ethylene glycol CH2OHCH2OH is ethane-1, 2-diol.
Real life uses :

Study the nature of chemicals.

Places to visit :

Chemistry laboratory.

Practical examples around us
Examples Explainations
ketones In general ketones (R-CO-R) take the suffix "-one" with an infix position number: CH3CH2CH2COCH3 is pentan-2-one. If a higher precedence suffix is in use, the prefix "oxo-" is used: CH3CH2CH2COCH2CHO is 3-oxohexanal.
What you learn in Theory:

An electrophile is a molecule that forms a bond to its reaction partner (the nucleophile) by accepting both bonding electrons from that reaction partner. Electrophilic reagents are Lewis acids.

What you learn in Practice:

A nucleophile is a molecule that forms a bond with its reaction partner (the electrophile) by donating both electrons for that bond. Nucleophiles are Lewis bases.

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