Question

isomers. Then, for each class, draw a pair of structures (in bond-line form) to clearly illustrate each class of isomer. Be sure to show proper spatial orientation where needed (often using dash/wedge bonds, or correct double-bond geometry). During your peer review: Did your peers draw correct examples? Suggest improvement if not.] A. Constitutional Isomers (or Structural Isomers) B. Conformational Isomers C. Configurational Isomers (or Stereoisomers) I. Enantiomers II. Diasteromers

For A, B, C and I and II. It just asks you to draw a pair of examples of the rype of ionomers.

Answer 1

A Congtituutional i8omereg :- (e1) ISomepg whieh have soMe mode eula forula but diffetent bonding Patten. a atomie orgamigation e.9 CH3-et2-e-CH3 CH3-CHe Moleeuta fofmula Same CHo but bold di fferemt, So this ore eI Patter

eon fomational ijonerg T80map uhieh ofe Can be CoNerted each Other by fotationl alaput omauy Sm9e badk C0ofotationH So the are eom for mational 8omr e. Gniguatiol al Igomeg Ctfeoisomes thax Comot be coNepted to each othe by otation about a Se bond

-CH3 H etlb eis) Car not Caverted to eaCh other, Sothey are Com FiBuYational T3omerg I. Enantiometg" each of a Paif of mleeuteg that or mitsor mogeg to each otheY Hoop foOH OH et3 Sothey afe enartiome D Diastfeomefg Stfeo i8omes that afe ot mtfroy images of one coko the and afe non- SuPepfSabLe ol one-amotho oH cold Not SufePmf mot mitor node Sable So the afe diatfeomerg