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can you answer and explain d-f?
![Draw the products of each reaction, and indicate the stereochemistry
where appropriate.
KOC(CH3)3
a.
-OTS
OH
b.
HBr
C.
Br2
SH
OTS
d.
KSH
PB13
e.
OH
f.
OH
TsCl
CH3CO2
pyridine
g.
HBr
h.
OH
i.
j.
k.
I.
S
Br
[1] NaOCH3
[2] H₂O
NaH
HI
(2 equiv)
S Na](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F39f6380b-55e3-47ff-8091-2f92e2b304db%2F8183af59-0e5e-452b-bff1-2347ca12084a%2Fm9ms2t_processed.png&w=3840&q=75)
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- What are the final products. Show stereochemistry if needed.Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides. One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(CzHs)3). 3SnCl4 + 4Al(C2H5)3 → 3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.160 L of SnCl4 (d= 2.226 g/mL) was treated with 0.346 L of triethylaluminum (Al(C2H5)3); d = 0.835 g/mL). What is the theoretical yield in this experiment (mass of tetraethylstannane, Sn(C2H5)4)? If 0.257L of tetraethylstannane (d= 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?Why does the melting point (70-71) above match neither the enantiomers’ nor the racemate’s? Does it mean that the substance is impure, or perhaps isn’t even ibuprofen at all? (Racemic mixture:75-77C, Enantiomer:52-53C)