557 cards
S N 1 products are ____
____ reactions lead to inversion of stereochemistry
S N 2 reactions lead to ____
The rate law for an S N 1 reaction is ____
The rate law for an S N 2 reaction is ____
A primary substrate will always go ____
A ____ substrate will always go S N 2
A tertiary substrate with a protic (or aprotic) solvent will go ____
A ____ substrate with a protic (or aprotic) solvent will go S N 1
This reaction will go ____
This reaction will go ____
S N 2 reactions prefer ____ substrates
S N ____ reactions prefer methyl and primary substrates
A methyl substrate cannot undergo an elimination reaction because elimination reactions create ____
A ____ substrate cannot undergo an elimination reaction because elimination reactions create double bonds between two carbons, C=C
Strong bases favor ____ reactions
____ favor E2 reactions
A secondary substrate with a protic solvent will go ____.
A secondary substrate with a ____ solvent will go S N 1.
A secondary substrate with an aprotic solvent will go ____.
A secondary substrate with an ____ solvent will go S N 2.
Polar ____ solvents are capable of hydrogen bonding .
Polar protic solvents are capable of ____.
Polar ____ solvents do not participate in hydrogen bonding.
Acetic acid is polar ____
DMSO is polar ____ .
____ use suffix – ol or prefix hydroxy -.
Alcohols use suffix – ____ -.
1º, 2º, and 3º alcohols are named according to the number of carbons attached to ____.
This is a ____ alcohol
____This is a primary alcohol
This is a ____ alcohol
____This is a secondary alcohol
This is a ____ alcohol
____This is a tertiary alcohol
This compound is known as a/an ____
____This compound is known as a/an phenol
The substituents on this benzene ring are in ____ position
The substituents on this benzene ring are in ortho position
The substituents on this benzene ring are in ____ position
____The substituents on this benzene ring are in meta position
The substituents on this benzene ring are in p____osition
____The substituents on this benzene ring are in para position
____ are conjugated cyclic diketones but are not aromatic .
Quin ones are conjugated cyclic diketones but are not ____.
Quin ones are ____ but are not aromatic .
____ are produced by reduction of quinones . Quinones are produced from phenols if you add an oxidizing agent. (OChem lit)
Hydroxy quinones are produced by ____. Quinones are produced from phenols if you add an oxidizing agent. (OChem lit)
Hydroxy quinones are produced by reduction of quinones . ____ are produced from phenols if you add an oxidizing agent. (OChem lit)
Hydroxy quinones are produced by reduction of quinones . Quinones are produced from ____ agent. (OChem lit)
____ is a biologically active quinone that acts as an electron acceptor in complexes I, II, and III of the electron transport chain
Ubiquinone is a biologically active ____ in complexes I, II, and III of the electron transport chain
When an alcohol is oxidized it becomes one of the following compounds:____
Treatment of an alcohol with pyridinium chlorochromate (PCC ) leads to the formation of a/an ____
Treatment of an alcohol with ____ leads to the formation of a/an aldehyde
-OH is a ____ leaving group
Alcohols can be converted to ____ to make them better leaving groups for nucleophilic substitution reactions
____ can be converted to mesylates or tosylates to make them better leaving groups for nucleophilic substitution reactions
Alcohols can be converted to mesylates or tosylates to make them ____ reactions
Aldehydes and ketones be protected by converting them into ____