7. Dimethyl sulfide contains a functional group that was not listed in lecture. Which functional group seen in lecture do you think its reactivity might resemble and why? (1-2 sentences) H3C-S-CH3

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7. Dimethyl sulfide contains a functional group that was not listed in lecture. Which functional group seen in
lecture do you think its reactivity might resemble and why? (1-2 sentences)
H3C-S-CH3
8. Identify and name all functional groups that are present in strychnine, a highly toxic alkaloid used as a
pesticide to kill rodents, and doxorubicin, a drug used as an antibiotic and cancer therapeutic. The bond-line
structure is shown below.
strychnine
O
O
OH
OH O
doxorubicin
OH
OH
NH₂
OH
Transcribed Image Text:7. Dimethyl sulfide contains a functional group that was not listed in lecture. Which functional group seen in lecture do you think its reactivity might resemble and why? (1-2 sentences) H3C-S-CH3 8. Identify and name all functional groups that are present in strychnine, a highly toxic alkaloid used as a pesticide to kill rodents, and doxorubicin, a drug used as an antibiotic and cancer therapeutic. The bond-line structure is shown below. strychnine O O OH OH O doxorubicin OH OH NH₂ OH
5. Redraw the following structures below in Lewis form, filling in all of the implied carbon atoms and hydrogen
atoms.
6. The following are the reagent, intermediate, and product in a reaction you will learn later in Organic
Chemistry.
a. Identify any formal charges that are missing from the structures.
b. Draw in all lone pairs.
c. Redraw the structures with all hydrogen atoms.
to t
OH ₂
Transcribed Image Text:5. Redraw the following structures below in Lewis form, filling in all of the implied carbon atoms and hydrogen atoms. 6. The following are the reagent, intermediate, and product in a reaction you will learn later in Organic Chemistry. a. Identify any formal charges that are missing from the structures. b. Draw in all lone pairs. c. Redraw the structures with all hydrogen atoms. to t OH ₂
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