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Compound with 2 triple bonds are called ____________.
diynes
Compounds with 3 triple bonds are called:
triynes
For radical halogenation, chlorination prefers to attach at the _________ substituted carbon. 
Least
For radical halogenation, chlorination: The major product is dependent on the number of _____________ ____________________.
like hydrogens
When there is a choice in numbering an enyne, __________ bonds receive lower numbers than __________ bonds. 
double; triple
Rank the stability of alkanes for radical halogenation from least to greatest with the choices given: 1. primary 2. secondary 3. tertiary  4. a methyl
methyl<primary<secondary<tertiary
Bromination produces the _______________ (more/least) substituted halogenated product as the major product. 
more
Compound containing both double and triple bonds are called __________.
enynes
Number an enyne starts from the end nearer the 1st _______ bond. 
multiple
What is the stereochemistry for an SN2 reaction?
100% inversion
In an SN2 reaction, the nucleophile attacks from the _________.
backside at 180 degrees away from the leaving group. 
E2 and SN2 reactions occur in _________ step(s).
one
What is the step called in the E2 and SN2 reaction?
the rate determining reaction
What determines the stereochemistry in an E2 reaction?
the anti periplanar transition state
SN2 reaction need what type of solvent?
polar, aprotic
E2 reaction need what type of solvent?
polar, aprotic
SN1 reaction need what type of solvent?
polar, protic
E1 reaction need what type of solvent?
polar, protic
What reactions form a carbocation
SN1 and E1

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