0244Pb3an-10.cwk (WP)

0244Pb3an-10.cwk (WP) - the answer. reverse D-A forward D-A...

Info iconThis preview shows pages 1–2. Sign up to view the full content.

View Full Document Right Arrow Icon
Answers to Problem 3, Chemistry 0244 - 2010 Short Answers: (a) (b) Yes you can, but it s really tricky. If you got this one, feel good: The reaction must be intramolecular. The only way to get it is to work backward - ask yourself “what would 1,3- cyclohexadiene give if it underwent a reverse Diels-Alder? The forward version must be
Background image of page 1

Info iconThis preview has intentionally blurred sections. Sign up to view the full version.

View Full DocumentRight Arrow Icon
Background image of page 2
This is the end of the preview. Sign up to access the rest of the document.

Unformatted text preview: the answer. reverse D-A forward D-A d. Now you have to use a ring compound as dienophile. e. This time it is the diene that must be cyclic. new bonds in bold f. Just use an acetylene as the dienophile. new bonds in bold g. new bonds in bold...
View Full Document

Page1 / 2

0244Pb3an-10.cwk (WP) - the answer. reverse D-A forward D-A...

This preview shows document pages 1 - 2. Sign up to view the full document.

View Full Document Right Arrow Icon
Ask a homework question - tutors are online