11 Intro To Organic Chem Flashcards
Hydrocarbons
Organic compounds which contain the elements carbon and hydrogen
Empirical formula
Simplest ratio of the number of atoms of the elements present in one molecule
Molecular formula
Actual number of atoms of the elements present in one molecule
Characteristics of a homologous series
- Same functional group
- Differs by a -CH2- group from one member to the next
- General formula
- Shows a gradual change in physical conditions
Alkane
C(n)H(2n+2)
Suffix: -ane
Prefix: alkyl-
Alkene
C(n)H(2n)
Suffix: -ene
Arene
Ar-R
Suffix: -benzene
Prefix: phenyl
Alkyl halide
R-X
Suffix: (nil)
Prefix: fluoro-/chloro-/
Aryl halide
Ar-X
Alcohol
R-OH
Suffix: -ol
Prefix: hydroxy-
Phenol
Ar-OH
Aldehyde
R/Ar -CH(O)
Suffix: -al
Prefix: oxo-
Ketone
Ar/R -(C=O)- Ar/R
Suffix: -one
Prefix: oxo-
Carboxylic acid
Ar/R-COOH
Suffix: -oic acid
Prefix: (nil)
Amide
Ar/R -CO(NH2)
Suffix: -amide
Prefix: (nil)
Amine
Ar/R -NH2
Suffix: -amine
Prefix: amino-
Nitrile
Ar/R -C三N
Suffix: -nitrile
Prefix: cyano-
Nitro compound
Ar/R -NO2
Suffix: (nil)
Prefix: nitro-
Amino acids
C(COOH)(NH2)
Ester
Ar/R -(C=O)O- Ar/R
Suffix: -oate
Prefix: (nil)
Hybridisation
The mixing of atomic orbitals in various combinations to give a set of hybrid orbitals of equivalent energy for covalent bonding with other atoms
sp^3 hybridisation
Mixing 1 s and 3 p valence orbitals
25.0% s character and 75.0% p character
sp^2 hybridisation
Mixing 1 s and 2 p valence orbitals
33.3% s character and 66.7% p character
sp hybridisation
Mixing 1 s and 1 p valence orbitals
50.0% s character and 50.0% p character
7 types of chemical reactions
- Addition
- Substitution
- Elimination
- Condensation
- Hydrolysis
- Oxidation
- Reduction
Nucleophile (Lewis base)
Electron pair donor and has a lone pair of electrons to be donated.
Can be negatively charged or neutral possessing a partial negative charge
Electrophile (Lewis acid)
Electron pair accepter and is electron-deficient
Can be positively charged or neutral possessing a partial positive charge
Homolytic fission
Each bonding atom takes 1 of the bonding electrons
Heterolytic fission
One of the bonding atoms takes both bonding electrons
Isomers
Same molecular formula but different arrangement of atoms in 3-dimensional space
Constitutional isomers
Same molecular formula but different structural formula
Chain isomers
Same functional group but different carbon chains
Positional isomers
Same carbon chain but different position of functional group
Functional group isomers
Differ in functional group
Stereoisomerism
Same molecular and structural formula, but different spatial arrangement of their atoms
Cis-trans isomers
- Restricted rotation about a covalent bond
- Two different groups/atoms attached to each carbon atom of that bond
Cis: identical groups on same side
Trans: identical groups on opposite sides
Enantiomers
Stereoisomers with non-superimposable mirror images
Chiral centres
Has 4 different groups (asymmetric)