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- The structure of 4 isomers of an aldotetrose carbohydrate are given. 1) select every structure that is a diastereomer of structure D A, B, or C? 2) select every structure that is a enantiomer of structure C D, B, or A? 3) select every structure that is a stereoisomer of structure D A, B, or CHow many chiral centers are there in the following compound? H. c=0 Н—с — оН НО — С — н Н—с —оН Н—с — он CH2OHDraw the meso isomer of 1,3-dihydroxycyclopentane (hydroxy = OH).
- This is an organic chemistry question. PLEASE SHOW STEP BY STEP! ALSO PLEASE INCLUDE ALL ELECTRON LONE PAIRS AND CHARGES FOR STRUCTURES IF NECESSARY!Draw and name the seven aldehydes and ketones with the formula C5H10O. Which are chiral?Determine the R/S configuration of each chiral center in the molecules shown below. (Do not include lone pairs as an attachment when identifying the chiral centers.)
- Tell how you could use a spectrometric method to distinguish geraniol (see Figure 2) from neral. CHO Neral1. How are each of the structures A-F related to structure X? They could be E (enantiomers), D (diastereomers), C (conformers), or I (identical). CH3 CH3 НО. CI- Br CH2OH CI CH3 CI CI Br HOH2C ОН HO Br 'CI HOH,C" OH Br CI HOH2Ċ CI X А. В C CI CI HO CI CI Br CH3 CI Br -CH3 H3C CH2OH ОН Br CI- ČH2OH HO "CH,OH D F ESub-part D, E, and F
- -2- 6. Draw the structure of Compound Y. 1. O3 CHIČCH,CH,CH,CH,CH, Compound Y 2 7n Hot2. H,N но PE PC In order to synthesize PC from PE, PE is reacted with three S-adenosylmethionine (SAM) molecules, producing three S-adenosylhomoserines (SAH). Draw the chemical reactions leading from PE to PC, including the important intermediates. Use the arrow formalism. Feel free to abbreviate certain groups with R to avoid excessive drawing, but make sure to draw the full substrates and products with all atoms at least once. H2N H2N N- он он N' NH2 NH2 KH Нон он OH OH S-adenosylmethioning S-adenosylhomoserineFill in the missing information for the following “road map” problem.
