Organic Chemistry Flashcards
What fo primary, secondary and tertiary alcohols oxidise into?
Primary: to aldehyde to acid
secondary: to ketone
tertiary: doesn’t oxidise
How to make an ionic equation?
Start with the half equations
- Remove all the oxygen, and balance with water
- Balance the H with H positive
- Balance the charge using the electrons
- Repeat for the other half equation
- Balance both equations and add them to cancel out the electrons
What’s an aldehyde?
Chain ENDS with a C connected to a double bond O and a single bond H
What’s a ketone?
A carbon not at the end of the chain that is connected to a double bond O
What’s a carbonyl?
C bonded to a double bond O and anything. The carbonyl is the CO, but it does not meant that it is not an aldehyde functional group
What’s a carboxylic acid?
Carbon chain ends with a C bonded to a double bond O and an OH
How do you oxidise a primary alcohol experimentally?
Fractional distillation to oxidise to aldehyde
Distill with reflux to acid- increases the time