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- How would you compound this order?Which is the anomeric carbon? I chose the one on the top left (substituent to carbon 5), but I believe it should be carbon actually in the cyclohexane, so my next guess would be bottom left (carbon 4). I'm a little confused.How many stereoisomers are possible for D-xylulose? A) 10 B) 6 C) 8 D) 4
- Put the following anions in order from most nucleophillic to least nucleophillic: Br- I- F- Cl-Below is Gulose in the open chain form: CHO H C-OH H C-OH HO C-H H- OH CH2OH Which of the following shows B-D-Gulose? A) B) CH2OH CH2OH OH ОН OH OH H H. OH OH H OH C) D) E) CH2OH H OH OH OH OH H CH2OH ČH2OH H H H. H. OH H. H. OH OH ÓH ОН H. -T -T I-1)Since bromelain is an endopeptidase, what types of bonds does it work on? 2)Since bromelain is an endopeptidase, what types of bonds does it work on?
- Why are plant steroids called sterols? Why are cholesterol and other steroids grouped under triterpenes but are not considered as true triterpenes?What are examples of polyiodides? Include their structure.Which of the following statements is TRUE for the enantiomer of the given monosaccharide? * ҫH,он H- -C-OH Но с -н H-C-OH ČH,OH It is an L-sugar that has opposite configuration around one carbon. It is a D-sugar that has opposite configuration around three carbons. O It is an L-sugar that has opposite configuration around three carbons. O It is a D-sugar that has opposite configuration around one carbon.