Mixing SbCl 3 and GaCl 3 in a 1 : 1 molar ratio (using liquid sulfur dioxide as a solvent) gives a solid ionic compound of empirical formula GaSbCl 6 . A controversy arises over whether this compound is ( SbCl 2 + ) ( GaCl 4 − ) or ( GaCl 2 + ) ( SbCl 4 − ) . (a) Predict the molecular structures of the two anions. (b) It is learned that the cation in the compound has a bent structure. Based on this fact, which formulation is more likely to be correct?
Mixing SbCl 3 and GaCl 3 in a 1 : 1 molar ratio (using liquid sulfur dioxide as a solvent) gives a solid ionic compound of empirical formula GaSbCl 6 . A controversy arises over whether this compound is ( SbCl 2 + ) ( GaCl 4 − ) or ( GaCl 2 + ) ( SbCl 4 − ) . (a) Predict the molecular structures of the two anions. (b) It is learned that the cation in the compound has a bent structure. Based on this fact, which formulation is more likely to be correct?
Solution Summary: The author explains how the molecular structures of SbCl_ 4- and
Mixing
SbCl
3
and
GaCl
3
in a
1
:
1
molar ratio (using liquid sulfur dioxide as a solvent) gives a solid ionic compound of empirical formula
GaSbCl
6
. A controversy arises over whether this compound is
(
SbCl
2
+
)
(
GaCl
4
−
)
or
(
GaCl
2
+
)
(
SbCl
4
−
)
.
(a) Predict the molecular structures of the two anions.
(b) It is learned that the cation in the compound has a bent structure. Based on this fact, which formulation is more likely to be correct?
Using the graphs could you help me explain the answers. I assumed that both graphs are proportional to the inverse of time, I think. Could you please help me.
Synthesis of Dibenzalacetone
[References]
Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below.
Question 1
1 pt
Question 2
1 pt
Question 3
1 pt
H
Question 4
1 pt
Question 5
1 pt
Question 6
1 pt
Question 7
1pt
Question 8
1 pt
Progress:
7/8 items
Que Feb 24 at
You do not have to consider stereochemistry.
. Draw the enolate ion in its carbanion form.
• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
⚫ Separate multiple reactants using the + sign from the drop-down menu.
?
4
Shown below is the mechanism presented for the formation of biasplatin in reference 1 from the Background and Experiment document. The amounts used of each reactant are shown. Either draw or describe a better alternative to this mechanism. (Note that the first step represents two steps combined and the proton loss is not even shown; fixing these is not the desired improvement.) (Hints: The first step is correct, the second step is not; and the amount of the anhydride is in large excess to serve a purpose.)
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