Assorted
What is the IUPAC name for anisole?
Methoxybenzene
How many different regions are there for alkynes on H NMR (and explain your answer)?
Only one: terminal alkynes are the only kind that would have a hydrogen attached to them
If an aromatic is not the priority in naming, how do you go about name it?
What reagent would I use if I want an alkyne to go to a cis alkene (with only adding hydrogens)?
Lindlar's Catalyst
What are the two kinds of products possible from a Diels-Alder reaction and which is the major?
Endo (major) and Exo
Are alkynes good electrophiles or nucleophiles? (Why?)
Good Nucleophiles, they have lots of electrons!
What are the four criteria for something to be aromatic?
1. Cyclic, 2. Planar, 3. Continuous overlapping P Orbitals, 4. Huckel's Rule (4N+2)
What are the four ways you can create a carbon-carbon bond?
R-Li, Grignard Reagents, F.C. Alkylation, F.C. Acylation
What are the five Electrophilic Aromatic Substitution Reactions?
1. Halogenation, 2. Nitration, 3. Sulfonation, 4. Friedel Craft Alkylation, 5. Friedel Craft Acylation
What were the two ranges of alkynes on IR spectra?
Terminal: 3300 | Internal: 2100-2250
Is quinoline (one of the reagents from Chapter 13) aromatic?
What reagent is used to turn a nitro group (NO2) into a primary amine (NH2)?
SnCl2 | HCl