Potassium acid phthalate, KNaC 8 H 4 O 4 , or KHP, is used in many laboratories, including general chemistry laboratories, to standardize solutions of base. KHP is one of only a few stable solid acids that can be dried by warming and weighed. A 0.3420-g sample of KNaC 8 H 4 O 4 reacts with 35.73 mL of a NaOH solution in a titration. What is the molar concentration of the NaOH? KNaC 8 H 4 O 4 ( a q ) + NaOH ( a q ) → KNaC 8 H 4 O 4 ( a q ) + H 2 O ( a q )
Potassium acid phthalate, KNaC 8 H 4 O 4 , or KHP, is used in many laboratories, including general chemistry laboratories, to standardize solutions of base. KHP is one of only a few stable solid acids that can be dried by warming and weighed. A 0.3420-g sample of KNaC 8 H 4 O 4 reacts with 35.73 mL of a NaOH solution in a titration. What is the molar concentration of the NaOH? KNaC 8 H 4 O 4 ( a q ) + NaOH ( a q ) → KNaC 8 H 4 O 4 ( a q ) + H 2 O ( a q )
Potassium acid phthalate,
KNaC
8
H
4
O
4
, or KHP, is used in many laboratories, including general chemistry laboratories, to standardize solutions of base. KHP is one of only a few stable solid acids that can be dried by warming and weighed. A 0.3420-g sample of
KNaC
8
H
4
O
4
reacts with 35.73 mL of a NaOH solution in a titration. What is the molar concentration of the NaOH?
KNaC
8
H
4
O
4
(
a
q
)
+
NaOH
(
a
q
)
→
KNaC
8
H
4
O
4
(
a
q
)
+
H
2
O
(
a
q
)
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.)
Applications and Investigations in Earth Science (9th 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