- Acetic acid
- Benzoic acid
- Stearic acid (long chain)
- All are readily reduced by LiAlH4?.
No category found.
- An alkoxide.
- An aldehyde.
- A carboxylate salt.
- A ketone.
- Oxygen
- Hydrogen
- Carbon dioxide
- Methane
- Propanal
- Propanone
- Propanoic acid
- Propene
- Preparing amines.
- Preparing alcohols.
- Increasing the carbon chain length.
- Decreasing the carbon chain length.
- It increases solubility by forming hydrogen bonds with benzene.
- It decreases solubility due to strong self-association.
- It has no effect on solubility.
- It makes them miscible with non-polar solvents.
- Increase acidity due to electron-donating effect.
- Decrease acidity due to electron-donating effect.
- Have no effect on acidity.
- Increase boiling point due to resonance.
- Carbonyl oxygen.
- Alpha-hydrogen.
- Hydroxyl group of the carboxyl function.
- Alkyl group.
- CO2? and H2?O
- CO and H2?O
- CO, CO2? and H2?O
- Formic acid
- Cooling the mixture.
- Adding a strong acid or base.
- Removing water from the reaction.
- Adding an oxidizing agent.
- Acid chloride
- Ester
- Amide
- Carboxylic acid
- An alkane with one less carbon.
- An alkene with twice the carbons.
- An alkane with double the carbons.
- An alcohol.
- POCl3? and HCl
- H3?PO3? and HCl
- PCl3? and HCl
- P2?O5? and HCl
- Phenols having a more stable phenoxide ion.
- Carboxylate ions having two equivalent resonance structures.
- Phenols having stronger hydrogen bonding.
- Carboxylic acids being non-polar.
- LiAlH4?
- NaBH4?
- DIBAL-H at low temperature
- H2?/Pd
- Water
- Ammonia
- A primary amine
- An alcohol
- Acetic anhydride is formed.
- Acetamide is formed.
- Ethylamine is formed.
- Acetonitrile is formed.
- It is a stronger reducing agent than other carboxylic acids.
- It cannot be oxidized further.
- It does not form esters.
- It is a weaker acid than acetic acid.
- Propanone
- Propane
- Propanal
- Calcium propanoate
