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Hydrogenation: H2,Ni high pressure/ H2,Pd - ANSWER-Reducing agent... Reduces
Alkynes and Alkenes - Alkanes
Aldehydes- primary alcohols
Ketones- secondary alcohols
Esters- two alcohols
Imine- amine
Amide- amine
Nitrile- primary amine
Nitro- amine
10% NaOH - ANSWER-Aldol Condensation
1.O3
2.Zn or Me2S
Or
1.03
2.H2O2 - ANSWER-1.Ozonolysis (oxidation of an alkene)
2.Hydrogen peroxide does further oxidation. Product = carboxylic acid
Carboxylic acid + 1. Alcohol 2. H3O+ (Work-up step) - ANSWER-Fischer esterification.
Carboxylic acid turns into an ester.
Alcohol + PCC - ANSWER-Primary alcohol + PCC = Aldehyde
Secondary alcohol + PCC = Ketone
, "Please stop oxidation at aldehyde & ketone"
Aldehyde or ketone + ethylene glycol and acid - ANSWER-Cyclic acetal
This serves as a protecting group for aldehydes or ketones. You can then react another
part of the molecule without touching the aldehyde or ketone part.
You deprotect the cyclic acetal and get your ketone or aldehyde back by acid and water.
R-MgBr - ANSWER-Grignards reagent
The purpose is to add carbons to a molecule.
Grignard workup - ANSWER-
Nitrile + 1. R-MgBr 2. H3O+ - ANSWER-Ketone
H3O+ (Acidic work-up step) - ANSWER-Purposes: a)acidic work-up step
b) acidic hydrolysis
c) Cleaves =N+ to =O
LAH (Lithium Aluminum Hydride) - ANSWER-STRONG REDUCING AGENT
Carboxylic acid - primary alcohol
All Carboxylic acid derivatives- primary alcohol
Aldehyde- primary alcohol(use NaBH4 rather)
ketone- secondary alcohol(use NaBH4 rather)
"Lets reduce everything"
CrO3 or H2CrO4 - ANSWER-Oxidizing agent
"Crap lets oxidize everything"
Ph3P=CH2 - ANSWER-WITTIG REAGENT