Sulfites are used worldwide in the wine industry as antioxidant and antimicrobial agents. However, sulfites have also been identified as causing certain allergic reactions suffered by asthmatics, and the FDA mandates that sulfites be identified on the label if they are present at levels of 10 ppm (parts per million) or higher. The analysis of sulfites in wine uses the “Ripper method” in which a standard iodine solution, prepared by the reaction of iodate and iodide ions, is used to titrate a sample of the wine. The iodine is formed in the reaction IO 3 − + 5I - + 6H + → 3I 2 + 3H 2 O The iodine is held in solution by adding an excess of I - , which combines with I 2 to give I 3 - . In the titration, the SO 3 2 − is converted to SO 2 by acidification, and the reaction during the titration is SO 2 + I 3 − + 2H 2 O → SO 4 2 − + 3I - + 4H + Starch is added to the wine sample to detect the end point, which is signaled by the formation of a dark blue color when excess iodine binds to the starch molecules. In a certain analysis, 0.0421 g of NaIO 3 was dissolved in dilute acid and excess NaI was added to the solution, which was then diluted to a total volume of 100.0 mL. A 50.0 mL sample of wine was then acidified and titrated with the iodine-containing solution. The volume of iodine solution required was 2.47 mL. (a) What was the molarity of the iodine (actually, I) in the standard solution? (b) How many grams of SO 2 were in the wine sample? (c) If the density of the wine was 0.96 g/mL, what was the percentage of SO 2 in the wine? (d) Parts per million (ppm) is calculated in a manner similar to percent (which is equivalent to parts per hundred). ppm = grams of component grams of sample ×10 6 ppm What was the concentration of sulfite in the wine, expressed as parts per million SO 2 2 ?
Sulfites are used worldwide in the wine industry as antioxidant and antimicrobial agents. However, sulfites have also been identified as causing certain allergic reactions suffered by asthmatics, and the FDA mandates that sulfites be identified on the label if they are present at levels of 10 ppm (parts per million) or higher. The analysis of sulfites in wine uses the “Ripper method” in which a standard iodine solution, prepared by the reaction of iodate and iodide ions, is used to titrate a sample of the wine. The iodine is formed in the reaction IO 3 − + 5I - + 6H + → 3I 2 + 3H 2 O The iodine is held in solution by adding an excess of I - , which combines with I 2 to give I 3 - . In the titration, the SO 3 2 − is converted to SO 2 by acidification, and the reaction during the titration is SO 2 + I 3 − + 2H 2 O → SO 4 2 − + 3I - + 4H + Starch is added to the wine sample to detect the end point, which is signaled by the formation of a dark blue color when excess iodine binds to the starch molecules. In a certain analysis, 0.0421 g of NaIO 3 was dissolved in dilute acid and excess NaI was added to the solution, which was then diluted to a total volume of 100.0 mL. A 50.0 mL sample of wine was then acidified and titrated with the iodine-containing solution. The volume of iodine solution required was 2.47 mL. (a) What was the molarity of the iodine (actually, I) in the standard solution? (b) How many grams of SO 2 were in the wine sample? (c) If the density of the wine was 0.96 g/mL, what was the percentage of SO 2 in the wine? (d) Parts per million (ppm) is calculated in a manner similar to percent (which is equivalent to parts per hundred). ppm = grams of component grams of sample ×10 6 ppm What was the concentration of sulfite in the wine, expressed as parts per million SO 2 2 ?
Sulfites are used worldwide in the wine industry as antioxidant and antimicrobial agents. However, sulfites have also been identified as causing certain allergic reactions suffered by asthmatics, and the FDA mandates that sulfites be identified on the label if they are present at levels of 10 ppm (parts per million) or higher. The analysis of sulfites in wine uses the “Ripper method” in which a standard iodine solution, prepared by the reaction of iodate and iodide ions, is used to titrate a sample of the wine. The iodine is formed in the reaction
IO
3
−
+ 5I
-
+ 6H
+
→
3I
2
+ 3H
2
O
The iodine is held in solution by adding an excess of
I
-
, which combines with
I
2
to give
I
3
-
. In the titration, the
SO
3
2
−
is converted to
SO
2
by acidification, and the reaction during the titration is
SO
2
+ I
3
−
+ 2H
2
O
→
SO
4
2
−
+ 3I
-
+ 4H
+
Starch is added to the wine sample to detect the end point, which is signaled by the formation of a dark blue color when excess iodine binds to the starch molecules. In a certain analysis, 0.0421 g of
NaIO
3
was dissolved in dilute acid and excess
NaI
was added to the solution, which was then diluted to a total volume of 100.0 mL. A 50.0 mL sample of wine was then acidified and titrated with the iodine-containing solution. The volume of iodine solution required was 2.47 mL. (a) What was the molarity of the iodine (actually, I) in the standard solution? (b) How many grams of
SO
2
were in the wine sample? (c) If the density of the wine was 0.96 g/mL, what was the percentage of
SO
2
in the wine? (d) Parts per million (ppm) is calculated in a manner similar to percent (which is equivalent to parts per hundred).
ppm =
grams of component
grams of sample
×10
6
ppm
What was the concentration of sulfite in the wine, expressed as parts per million
SO
2
Transmitance
3. Which one of the following compounds corresponds to
this IR spectrum?
Point out the absorption band(s) that helped you
decide.
OH
H3C
OH
H₂C
CH3
H3C
CH3
H3C
INFRARED SPECTRUM
0.8-
0.6
0.4-
0.2
3000
2000
1000
Wavenumber (cm-1)
4. Consider this compound:
H3C
On the structure above, label the different types of H's
as A, B, C, etc.
In table form, list the labeled signals, and for each
one state the number of hydrogens, their shifts, and the
splitting you would observe for these hydrogens in the ¹H
NMR spectrum.
Label
# of hydrogens
splitting
Shift (2)
Physics for Scientists and Engineers: A Strategic Approach, Vol. 1 (Chs 1-21) (4th Edition)
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Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell