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Alkene functional group
-ene
C=C
Alcohol functional group
-ol
hydroxy-
C-OH
Haloalkane functional group
chromo-
bromo-
iodo-
C-halogen
Aldehydes functional group
-al
C-H
()
H
Ketones Functional Group
-one
oxo-
C=O
Carboxylic acid functional group
-oic acid
Nitriles functional group
-nitrile
amines functional group
-amine
amino-
Molecular formula
Formula that gives the actual number of atoms of each element of one molecule
Empirical Formula
Formula that gives the simplest ratio of atoms of each element in a compound
Hydrocarbon definition
Organic compounds composed of exclusively carbon and hydrogen: E.g. C4H10 (Butane)
Isomers definition
Compounds with the same molecular formula but different structural formula. (Structural Isomer)
Substitution reaction
Where one atom or a group of atoms is substituted for another.
2 reactants → 2 products
reactant “similarly natured”
Addition reaction
Two substances react together to form a single substance.
usually involves double or triple bond.
2 reactant → 1 product
reactant added to unsaturated molecule to make a saturated one.
Elimination reaction
Removal of a molecule from a saturate one to make an unsaturated molecule
1 reactant → 2 products
Homolytic fission (same)
bonding electrons equally sgared between two atoms.
Free radicals formed are very reactive.
forms two neutral atoms
Heterolytic fission (different)
One of the bonded atoms takes both of the bonding electrons to form an anion.
Most electronegative element takes both electrons.
forms one negative, one positive
Electronegative definition
An atom's tendency to attract a pair of bonding electrons towards itself
Free radicals
Unpaired electrons
strong tendency to pair up with an electron from another substance
Nucleophiles (nucleus lovers)
Electron pair donors.
often negative ions with lone pair of electrons
: colon represents pair of electrons
Electrophiles (electron lovers)
Electron pair acceptors.
must have vacancy for a lone pair of electrons to form new bond.