Organic Chemistry

Science

Math

Humanities

... and beyond

Socratic Meta
Featured Answers

Topics

Why are secondary and tertiary amines less soluble than primary amines of similar molecular size?

1 Answer

Apr 29, 2015

Secondary and tertiary amines are less soluble in protic solvents because they can form less hydrogen bonds with the solvent

Related questions

What are the steps used to name an ester?
What do the functional groups determine?
How can I draw the following aldehydes and ketones: hexanal, heptan-3-one, 3-methyloctanal?
How can I draw the following carboxylic acids: butanoic acid, 2-methylpentanoic acid,...
How can I draw the following ethers: 1-propoxypentane, 2-ethoxybutane, 1-methoxy-4-chlorohexane,...
How can I draw the following esters: ethyl butanoate, pentyl propanoate, propyl 3-ethylhexanoate?
How can I draw the following amides: N-ethylbutanamide, N-propylpentanamide, N,3-dimethylhexanamide?
Why do amines generally have lower boiling points than alcohols of comparable molar mass?
In some cuisines, fish recipes include lemon garnish or a vinegar sauce such as sweet and sour...
Which functional groups would form hydrogen bonds with neighbouring molecules?

See all questions in Naming Functional Groups

Impact of this question

9275 views around the world

You can reuse this answer
Creative Commons License