Substituents Reactivity
S and E Reactions
The Distillery
REACTION
100

This is the most activating group on an aromatic ring.

What is a substituent with a lone pair.  But not halogens

100
These are reactions that lose something.
What is E1 and E2?
100
This reaction is used in alcohol synthesis and has an organomercury intermediate.
What is oxymercuration?
100

What method makes xylene

What is Friedel Craft Alkylation

200

SO3H is this kind of director.

What is meta?

200
In this reaction a strong base is needed.
What is E2?
200
This reaction uses BH3/THF with H2O2, OH-.
What is hydroboration?
200

The reagents needed to produce chlorobenzene

What are: Cl2 , AlCl3 and Benzene

300
Alcohol is a ____ ____ director.
What is activating o-p?
300
These two types of reactions form carbocations.
What is SN1 and E1?
300
The use of OsO4/pyridine and NaHSO3/H2O makes this.
What is a syn diol?
300

These reactions make a good leaving group.

what are halogens

400

Benzene is more activating than 

What is Nitrobenzene  or any substituted benzene with a deactivating group?

400
This reaction has an inversion of stereochemistry.
What is SN2?
400
Hitting a ketone with this will makes a secondary alcohol.
What is NaBH4 and H2O?
400

Toluene Oxidation with KMnO4 yields this

What is a benzoic acid? or a carboxylic acid

500
Of -OR and -COR, this is the more activating.
What is -OR?
500
This reaction yields a racemic mixture.
What is SN1?
500
The use of mCPBA(epoxide) and H3O+ makes this.
What is a trans diol?
500

The turning of an alcohol into an alkene is an example of this.

What is dehydration?

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