Description

replacement of group by another
donates a pair of electron to form a chemical bond in relation to a reaction
a molecular fragment that departs with a pair of electrons in a reaction
reaction where energy is transferred to the surroundings
reaction where energy is taken in from the surroundings
represents transfer of a pair of electrons
the type of nucleophilic substitution SN2 reaction involves in.
the type of stereochemistry form SN2 reaction leads to.
the intermediate formed in SN1 reaction
composition of dextrorotatory and laevorotatory forms of a compound in equal proportion
which is the rate determing step in SN1 reaction
the elemination reaction where by removal of the H forms the more substituted (more stable) alkene
process where more than one orientation is possible in a product
bases which leads to more substituted alkene
compound containing carbon to carbon double bond
number of intermediate cabocations formed in addition reaction involving an unsymmetrical alkene
first step in the addition reaction between an alkene and hydrochloric acid (HCl)
the rule that state that the more substituted halide is formed from the addition of H-X to an alkene
second step in radical reaction
a specie with an unpaired electron
type of dihalides molecular bromide and chlorine give rise to when added to alkenes
arrow indicating the movement of a single electron
fission involved the splitting of a bond to produce particles which are the same with both having a single unpaired electrons
most stable form in radical stability due to resonance
which good bases favours Elimination (E1) reaction

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