23. In this dimethyl sulfate (DMS) chemical probing reaction, alkylation occurs at the N1 of adenosine or the N3 of cytidine to disrupt W-C pairing. Use electron pushing arrows (in at least 2 steps) to draw the chemical mechanism for how either the A or C nucleobases become methylated (do not draw ribose/backbone moieties). Indicate the charge of the methylated nitrogen. DMS N-H- H3C CH3 A N---. N=/1 H. N-H- R

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23. In this dimethyl sulfate (DMS) chemical probing reaction, alkylation occurs at the
N1 of adenosine or the N3 of cytidine to disrupt W-C pairing. Use electron pushing
arrows (in at least 2 steps) to draw the chemical mechanism for how either the A or C
nucleobases become methylated (do not draw ribose/backbone moieties). Indicate
the charge of the methylated nitrogen.
DMS
N-H-
H3C
CH3
A N---.
N=/1
H.
N-H-
R
Transcribed Image Text:23. In this dimethyl sulfate (DMS) chemical probing reaction, alkylation occurs at the N1 of adenosine or the N3 of cytidine to disrupt W-C pairing. Use electron pushing arrows (in at least 2 steps) to draw the chemical mechanism for how either the A or C nucleobases become methylated (do not draw ribose/backbone moieties). Indicate the charge of the methylated nitrogen. DMS N-H- H3C CH3 A N---. N=/1 H. N-H- R
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