1) Why do we use H3PO4 instead of
H2SO4 as a catalyst for the synthesis of
cyclohexene?
2) Why do we use H3PO4 instead of HCl as a
catalyst for the synthesis of cyclohexene?
3) What alkene(s) would be produced on dehydration of each of
the following alcohols? If more than one product is possible, use
Zaitsev’s rule to predict which product would be formed in greater
amounts.
a) 2-methylcyclohexanol
b) 2,2-dimethylcyclohexanol
c) 1,2-cyclohexanediol
Problem Set for “Cyclohexene”
1. Why do we use H3PO4 instead of
H2SO4 as a catalyst for the synthesis of
cyclohexene
2. Why do we use H3PO4 instead of HCl as a
catalyst for the synthesis of cyclohexene?
3. What alkene(s) would be produced on dehydration of each of
the following alcohols? If more than one product is possible, use
Zaitsev’s rule to predict which product would be formed in greater
amounts.
(a) 2-methylcyclohexanol
(b) 2,2-dimethylcyclohexanol
(c)...
Why do we use Saccharomyces Cerevisiae instead of Escherichia
coli in a lab study conducted to determine COX activity (cytochrome
oxidase), what is the advantage in doing so?
Why do we model a competitive firm with assumptions that seem to
be unrealistic? Why do we see that marginal cost tends to increase
with each unit of output? Why do we observe a U-shaped Average Cost
Curve? Why is it the Marginal Revenue equal to the Price? What does
it mean that the Marginal Revenue curve is a flat horizontal curve?
Why do we assume that companies are profit-maximizing institutions?
After all, they may care about something else besides...
Use SPSS® to check your mock data for the following: •
Assumptions of normality (Shapiro-Wilk) • Homogeneity of variance
(Lavene) • Outliers • Skewness/Kurtosis Complete each of the
associated tasks below: 1) Create a series of tables that depict
your results. Do not simply paste your output from SPSS®;
0.00
21.00
0.00
21.00
0.00
42.00
0.00
18.00
0.00
15.00
0.00
24.00
0.00
36.00
0.00
36.00
0.00
18.00
0.00
24.00
0.00
30.00
0.00
39.00
0.00
21.00
0.00
15.00
0.00
51.00
0.00...
Why do we use chlorosulfonic acid for sulfanilamide from
acetanilide instead of the
SO3/H2SO4 combination? (Think
about the second step of the reaction)