(1) In case of paraldehyde I see 3 similar chiral carbons. So I divided it into 2 subcases
-two methyls above the plane and one below the plane
-all three above the plane
so, that makes it 2. When I looked this up on Wikipedia I found this,
can,(1) and (4) not be obtained by simply ring flipping, doesn't that make them conformers? Do I need to count them separately in my count of stereoisomers?
this according to me should have 4 stereosiomer(not including conformers) can someone confirm this answer? Are there any more im missing out?