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A Word is Worth a Thousand Pictures

Teacher: Das Thamattoor
Across
Reaction of KMnO4 or OsO4 with alkene leads to this.
Device for determining orbitals.
A stable enol.
This many electrons could make it aromatic.
From reduction of nitriles or amides with lithium aluminum hydride.
This kind of cleavage leads to a radical.
An ether.
This contains two adjacent double bonds.
Control in effect when 1,2-addition is favored over 1,4-addition.
This acetic ester can be formed from a Claisen condensation.
An aldehyde.
Reagent for epoxidation.
Preferred diene conformation in a Diels-Alder.
This describes ketones and enols.
This is not reduced by sodium borohydride.
Hydration of 2-butyne gives this compound.
Radical Initiator.
Ortho-para director.
These are useful protecting groups.
Used in Birch reduction.
Strong nonnucleophilic base (abbr.)
Way to make aldehydes, ketones, and carboxylic acids from alkenes.
Place for posting course material.
This is a polyamide.
The kind of rotation in a thermal 4n electrocyclic reaction (abbr.)
Nucleophilic aromatic substitution requires these in the ortho and para position(s) (abbr.)
Catalyst required for a Fischer esterification.
This mediates amide formation (abbr.)
The position to which a cyano group directs.
Zn-Hg/HCl will convert benzaldehyde to this compound.
A common reaction of radicals.
Compounds of this element are used in the Sandmeyer reaction.
Starting material for a Beckmann Rearrangement.
A beta-hydroxyaldehyde is called this.
Down
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.
I love dienes!
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.
1,3-Cyclobutadiene.
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.
Friedel-Crafts catalyst.
Charged.
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.
This is how benzene is.
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.
A cyclic ester.
Deactivator.
You need this acid to make a diazonium compound.
Used with rotovaps.
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.