Reagents With Organic Chem Flashcards
Elimination of an alcohol gives what product, using what reagent
Reagent =Concentrated acid e.g. H2SO4, H+
Product = alkene
Hydration of an alkene forms
what product,
using what reagent
Product=alcohol
Reagent= dilute acid (H2SO4 + H2O ; H3O+)
How do we ensure halohydrin formation instead of dihalogenation?
Which 2 reagents allows this?
NBS (N-Bromo succinimide) and water
Same time
What 4 metal catalysts do we use in hydrogenation and they are often with carbon
Pd, Pt, Ni, Fe
Which catalyst with H2 on reacts with alkynes .
It is therefore called……
Lindlar
Chemoselective
Sn1 reaction only work with what alcohols
3°
What 2 reagents dont go through carbocation to form halogenoalkanes from alcohols
- SOCl2 (thionyl chloride)
2. PBr3 (phosphorus tribromide)
What are 2 ways to make carbonyl compounds
- Oxidation of 1° and 2° alcohols
2. From ozonolysis of alkenes
What reagent can be used by both
1° alcohol to form an aldehyde
and
2° alcohols to form a ketone
PCC , THF (together)
What reagent can only be used by 2° alcohols to form an aldehyde
Jones reagent with water
CrO3, H2SO4 and H2O same time
If you added Jones reagent to a 1° alcohol what would you get instead of a carbonyl
A carboxylic acid
What are the 5 reactions of aldehydes and ketones and their products
- Grignard reactions = alcohol
- Acetal formation = acetal
- Imine formation= imine
- Reduction = alcohol
- Cyanohydrin formation= cyanohydrin formation
What do you have to add to a halogenoalkane to form a grignard reagent
Mg and THF
What do you have to add to a carbonyl group to get an imine (2)
1° anine and H3O+ at same time
What are our 2 reducing agents for carbonyl compounds to form alcohols
- LiAlH4 (LAH) lithium diminium hydride
2. NaBH4 sodium borohydride