Organic Chemistry
60 terms · page 3 of 3
Organic Chemistry
Organic Chemistry
Dimensionless
The study of the structure, properties, composition and reactions of carbon-containing compounds.
Oxidation of Alcohols
Organic Chemistry
Dimensionless
The conversion of alcohols to carbonyl compounds or carboxylic acids by removal of hydrogen.
R–CH₂OH → RCHO → RCOOH
Phenol
Organic Chemistry
Dimensionless
A compound in which a hydroxyl group is bonded directly to an aromatic ring.
C₆H₅–OH
Position Isomerism
Organic Chemistry
Dimensionless
Structural isomerism arising from a functional group occupying different positions on the same carbon skeleton.
Racemic Mixture
Organic Chemistry
degrees
An equimolar mixture of two enantiomers, which shows no net optical rotation.
50:50 (+) and (−)
Resonance Effect
Organic Chemistry
Dimensionless
The delocalisation of pi or lone pair electrons through a conjugated system, altering electron density at distant atoms.
−M and +M effects
Saturation and Unsaturation
Organic Chemistry
Dimensionless
The distinction between compounds containing only single bonds and those containing multiple bonds or rings.
DoU = (2C + 2 + N − H − X)/2
SN1 Reaction
Organic Chemistry
s⁻¹
A two-step nucleophilic substitution proceeding through a carbocation intermediate.
rate = k[substrate]
SN2 Reaction
Organic Chemistry
L/(mol·s)
A single-step nucleophilic substitution in which bond formation and bond breaking occur simultaneously.
rate = k[substrate][nucleophile]
Stereoisomerism
Organic Chemistry
Dimensionless
Isomerism in which molecules have identical connectivity but differ in the spatial arrangement of their atoms.
Structural Isomerism
Organic Chemistry
Dimensionless
Isomerism in which the compounds differ in the order in which their atoms are connected.
Zaitsev's Rule
Organic Chemistry
Dimensionless
In an elimination reaction, the major product is usually the more highly substituted and therefore more stable alkene.