R3.2 Electron transfer reactions

0.0(0)
Studied by 0 people
call kaiCall Kai
Locked
learnLearn
examPractice Test
spaced repetitionSpaced Repetition
heart puzzleMatch
flashcardsFlashcards
GameKnowt Play
Card Sorting

1/8

encourage image

There's no tags or description

Looks like no tags are added yet.

Last updated 3:50 AM on 7/8/26
Name
Mastery
Learn
Test
Matching
Spaced
Call with Kai
Chat

No analytics yet

Send a link to your students to track their progress

9 Terms

1
New cards

How do primary alcohols form aldehydes?

Through partial oxidation by distillation and heat

Excess alcohol used and aldehyde distilled as it’s produced

2
New cards

What can primary alcohols form upon oxidation?

Aldehyde (from heat and distillation)

Carboxylic acid (heat under reflux)

3
New cards

What is distillation?

Used to separate components of a mixture with different boiling points

4
New cards

How is distillation used upon the formation of aldehydes?

Aldehydes have weaker intermolecular forces than alcohols (and carboxylic acids)→ lower boiling points→they evaporate after heating and rises up the fractioning column→condensates to form liquid

5
New cards

True or false: primary alcohols can be converted to carboxylic acids directly

True. Complete oxidation as an excess oxidising agent is used and heated under reflux

6
New cards

How does reflux condenser work?

Prevents loss of solvent in mixture

Vapours rise up column, condense and flow back down

7
New cards

What’s formed after oxidation of secondary alcohol?

Ketones (heated under reflux)

8
New cards

What’s formed after oxidation of secondary alcohol?

Ketones (heated under reflux)

9
New cards

What are tertiary alcohols converted to upon oxidation?

Nothing, they can’t oxidise