Oil and water don't do this.
These two are located on adjacent atoms.
Glassware/solvent for Grignard and many organometallic reactions.
May be associated with MS.
Metal used to aid bromination of benzene.
An example of a reaction controlled by orbital symmetry.
This can help make a cis-alkene.
Number of steps in a concerted reaction.
Anti-Markovnikov addition of HBr is an example of this type of reaction.
This carbene is stereospecific in its addition to double bonds.
Hybridization of the central carbon in a ketene.
Example of halogenating a benzene ring (abbr.)
Primary amines react with ketones/adehydes to form these compounds.
This chloride is good for converting OH to Cl.
Might want to do this before taking the final.
Would give this and a leg to do well in the exam.
Beta-ketoacids tend to lose this.
Average, or someone who writes really nasty OChem tests.
Reaction of alkyne with sodium and ammonia gives this alkene.
This acid group is good for blocking.
Weird intermediate that rhymes with I'm fine.
Essential for a Wittig reaction.
Linear system of three p orbitals that are lined up the same way
Two double bonds separated by a single bond.
Lithium aluminum hydride can help convert a carboxylic acid to this.
NBS works on this position.
You might do this when you spot an easy problem on the OChem test.
This is found in aldehydes, ketones, acids, esters, amides, and anhydrides.
You need this acid to make a diazonium compound.
Position attacked by a nucleophile in aromatic substitution..
You might need this to cool your reaction.
You need at least this many alpha protons to carry out a Claisen Ester Condensation.
This group is formed by dehydrating a primary amide.