24. C2H5-S-C2H5 is an example of O thiols O thioethers thioaldehydes 25. All amino acids, except , are optically active due to the presence of an asymmetric carbon atom in the molecule. Because of the asymmetric carbon, they form D- and L-enantiomers. O valine O leucine O glycine 26. electron-rich species (nucleus-seeking): region of high electron density. O Nucleophile O Electrophlle

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter26: Biomolecules: Amino Acids, Peptides, And Proteins
Section26.SE: Something Extra
Problem 34AP: Using both three- and one-letter codes for amino acids, write the structures of all possible...
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O Organic Chemistry Lecture Fina
E Organic Che
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IOEWIKwgzP
YH3CIVMwSTIcirq7vnq7w/viewform?edit requested%3Dtrue#settings
24. C2H5-S-C2H5 is an example of
thiols
thioethers
thioaldehydes
25. All amino acids, except , are optically active due to the presence of an
asymmetric carbon atom in the molecule. Because of the asymmetric
carbon, they form D- and L-enantiomers."
valine
leucine
glycine
26.
electron-rich species (nucleus-seeking), region of high
electron density. *
O Nucleophile
Electrophle
Transcribed Image Text:O Organic Chemistry Lecture Fina E Organic Che Dashboard IOEWIKwgzP YH3CIVMwSTIcirq7vnq7w/viewform?edit requested%3Dtrue#settings 24. C2H5-S-C2H5 is an example of thiols thioethers thioaldehydes 25. All amino acids, except , are optically active due to the presence of an asymmetric carbon atom in the molecule. Because of the asymmetric carbon, they form D- and L-enantiomers." valine leucine glycine 26. electron-rich species (nucleus-seeking), region of high electron density. * O Nucleophile Electrophle
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