{[ promptMessage ]}

Bookmark it

{[ promptMessage ]}

Chem 140A Lauren mt2 practice key

Chem 140A Lauren mt2 practice key - The meso stereoisomer...

Info iconThis preview shows pages 1–4. Sign up to view the full content.

View Full Document Right Arrow Icon
Background image of page 1

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

View Full Document Right Arrow Icon
Background image of page 2
Background image of page 3

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

View Full Document Right Arrow Icon
Background image of page 4
This is the end of the preview. Sign up to access the rest of the document.

Unformatted text preview: The meso stereoisomer of 1,3-dichlorocyclohexane The enantiomer of(1R, 3R)-djmethylcyclopentane Cl SCHs '1 CH3 A diastereomer of trans-l ,2-dimethylcyclopropane The most stable chair form of 1,3,5-u‘imethylcyclohexane CH3 CH3 unwell; CH3 A compound of molecular formula C3H14 containing a fused ring system <:O there are more possibilities draw valid resonance forms of the following molecules. a E + CH3 No Raactim Br GB; + Na] draw the mechanism for the following reaction OCHZCH3 ©><3r CH3CH20H ©><++: : (' B1 >+ :+ HOCHZCH3 +QCH2CH3 Draw all of the isomers, including stereoisomers, of CngClz which contain a cyclopentane ring. Label any compounds which are meso stereoisomers and label pairs of enantiomers. C1 C1 E5 g} (Swo— 0—0 C] enantiomers 111630 g3] \ Cl draw a reasonable mechanism for the reaction below. be sure to account for the stereochemical outcome OH H OSOzCHg, Base ”Mu. polar aprotic solvent a single enantiorner a single enanfiomer H +6 §CH3 H + _ 8N2 with inversion 0802CH3 of configuration CHs ...
View Full Document

{[ snackBarMessage ]}