10&20. Organic Flashcards
Alkane
-ane
CH2
Alkene
-ene
-CH=CH-
Alkenyl
Alkyne
-yne
-C≡C-
alkynyl
Halogenoalkane
Chloro, bromo etc
-F, -Cl etc
Halogen
Ether
-oxy-
-O-
ether
Alcohol
-ol
OH
Hydroxyl
Aldehyde
-al
-CHO
Carbonyl
Ketone
-one
-CO-
Carbonyl
Ester
-oate
-COO-
Ester
Carboxylic acide
-oic acid
-COOH
carboxyl
Amine
-amine
-NH2
Amino
Amide
-amide
CONH2
Carboxymide
Nitrile
-nitrile
-CN
Nitrile
Arene
-benzene or phenyl-
Phenyl
Primary, secondary and teritiary molecules
A primary carbon in bonded to just one hydrocarbon chain, a secondary to two and a tertiary to three.
Structural isomers
= two or more compounds that have the same molecular formula but a different structural formula.
Saturated compound
Molecule with no double or triple bonds
Free radical
an uncharged species that has an unpaired valence electron
Electrophile
an electron-deficient species that can accept electron pairs from a nucleophile.
Markovnikov’s rule
when hydrogen halides add to asymmetrical alkenes, the hydrogen atom always adds to the carbon atom that already has the most hydrogen atoms bonded to it.
How can an aldehyde be formed?
Oxidation of an alcohol
Reduction of carboxylic acid
How can a carboxylic acid be formed?
Oxidation of an aldehyde
Oxidation of an alchohol (via an aldehyde)
How can an alcohol be formed?
Addition of an alkane
Substitution of a halogenoalkane
Reduction of a ketone
Reduction of an aldehyde
How can a ketone be formed?
Oxidation of an alcohol