10.1 Fundamentals of organic chemistry Flashcards
define catenation
CATENATION: C ability to form chains and rings - vast number of carbon compounds
Dustinguish saturated vs unsaturated

Distinguish aliphatics vs arenes

Distinguish electrophile vs nucleophile

Dinstinguish addition vs substitution vs addition elimination reactions

Types of bond breaking

Representation of moving e in reaction mechanisms

Alkane general formula
CnH2n+2
General formula of alcohols
CnH2n+1OH
Features of a homologous series

Types of chemical formulas and their characteristics
- full structural
- condensed structural
- stereochemical: with 3D projections

Steps of naming an organic compound
- Identify longest C chain
- Identify functional groups (what the compound is)
- Identify side chains
- Construct the name

define structural isomers
STRUCTURAL ISOMERS: molecules that have the same molecular formula but different structural arrangements of the atoms
How are primary, secondary, tertiary compounds identified
Primary - 1 C atom bonded to central
Secondary - 2 C atoms bonded to central
Tertiary - 3 C bonded to central

Explain arenes
Arenes: compounds derived from benzene, form aromatics branch - contain the phenyl group

Facts on benzene
- no isomer
- highly unsaturated - ratio of C and H the same - C6H6
- IUPAC: 1,3,5 - cyclohexatriene
- very stable due to: equal bonds 120, resonance of delocalised pi e - distributed equaly - minimises repulsion
- more likely substitution than addition - addition energetically not favoured - disrupts delocalised e cloud

Increase in boiling point according to functional group
