EDTA can be found as an ingredient in cosmetics and personal care products. Give the reason...
EDTA can be found as an ingredient in cosmetics and personal care products. Give the reason for the addition of EDTA in cosmetics and the reaction involved. (5marks)
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EDTA can be found as an ingredient in cosmetics and personal
care products. Give the reason...
13) the addition of this to butadiene can give 2 different products. The major product depends...
13) the addition of this to butadiene can give 2 different products. The major product depends on reaction Conditions the reaction has 2 steps", separated by a short-lived intermediate КСІ Wa A Co - tabel the products on the ran coordinate diagram, * A is the more stable product, - which product is formed faster? - Compare the activation energies of the 1st step.
Show the following mechanism for the reaction below. Give all the possible products that can be...
Show the following mechanism for the reaction below. Give all the possible products that can be formed plus circle and label the major and minor products. (6 pts) H2SO4 MeOH
Give all possible products from the following mixed aldol reaction and show how they can be...
Give all possible products from the following mixed aldol reaction and show how they can be formed. 0 H Н,О н
3. Give the structures of the two products for addition reaction of HCI to 3-methyl-1-pentene (1...
3. Give the structures of the two products for addition reaction of HCI to 3-methyl-1-pentene (1 point), Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) OH
Bonus 3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene...
Bonus 3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene (1 point). Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) Он Br
A synthetic trap occurs when a reaction can give more than one desired product. For the reaction below, draw the stuctures of the two organic compounds that were actually formed following addition of CH3CH2Li and subsequent aqueous acid workup.
A synthetic trap occurs when a reaction can give more than one desired product. For the reaction below, draw the structures of the two organiccompounds that were actually formed following the addition of \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{Li}\) and subsequent aqueous acid workup.Draw the structures of the two organic compounds which were actually isolated so that all eleven carbons involved in the reactions are accounted for in your answer.
4. Enol ether 10 can be hydrolyzed under acidic conditions to give products 11 and 12....
4. Enol ether 10 can be hydrolyzed under acidic conditions to give products 11 and 12. acidic ER aqueous conditions + HOR' a) Draw a mechanism for the enol ether hydrolysis reaction. b) The rates for the hydrolysis of enolether 10 were determined. Find below a graph with the reaction rates in H20 and D20 in the pH range of 3 to 4.5 (o for the reaction in H20 and for the reaction in D-0). Designate the slowest step in...
35. Carbon monoxide and hydrogen can react under different conditions to give different products. One system...
35. Carbon monoxide and hydrogen can react under different conditions to give different products. One system produces methyl alcohol, CH 3O H (g), when CO and H2 react in the presence of a suitable catalyst. a. At 227°C, after the reaction has reached equilibrium, the partial pressures of CO, H 2, and CH 3O H are 0.702 atm, 1.75 atm, and 0.0134 atm, respectively. Calculate K c for the reaction at 227°C. b.What is the K c for the decomposition...
a) Which products (shown above) from reaction 3 can react with HCl in an acid-base reaction?...
a) Which products (shown above) from reaction 3 can react with
HCl in an acid-base reaction? Show the mechanism for this acid-base
reaction and give the structures that would result from the
protonation of these products. Which phase (organic or aqueous)
would these protonated products be soluble in?
b) Which phase (organic or aqueous) would the
p-methylacetanilide be found in?
In step 5 of reaction 3, the reaction mixture containing the products shown below in ethyl acetate is extracted twice...
a) Which products (shown above) from reaction 3 can react with HCl in an acid-base reaction?...
a) Which products (shown above) from reaction 3 can react with
HCl in an acid-base reaction? Show the mechanism for this acid-base
reaction and give the structures that would result from the
protonation of these products. Which phase (organic or aqueous)
would these protonated products be soluble in?
b) Which phase (organic or aqueous) would the
p-methylacetanilide be found in?
c) Why did we have to use hot ethanol for the
recrystallization?
d) Why did we have to cool the...
13) the addition of this to butadiene can give 2 different products. The major product depends on reaction Conditions the reaction has 2 steps", separated by a short-lived intermediate КСІ Wa A Co - tabel the products on the ran coordinate diagram, * A is the more stable product, - which product is formed faster? - Compare the activation energies of the 1st step.
Show the following mechanism for the reaction below. Give all the possible products that can be formed plus circle and label the major and minor products. (6 pts) H2SO4 MeOH
Give all possible products from the following mixed aldol reaction and show how they can be formed. 0 H Н,О н
3. Give the structures of the two products for addition reaction of HCI to 3-methyl-1-pentene (1 point), Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) OH
Bonus 3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene (1 point). Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) Он Br
4. Enol ether 10 can be hydrolyzed under acidic conditions to give products 11 and 12. acidic ER aqueous conditions + HOR' a) Draw a mechanism for the enol ether hydrolysis reaction. b) The rates for the hydrolysis of enolether 10 were determined. Find below a graph with the reaction rates in H20 and D20 in the pH range of 3 to 4.5 (o for the reaction in H20 and for the reaction in D-0). Designate the slowest step in...
a) Which products (shown above) from reaction 3 can react with
HCl in an acid-base reaction? Show the mechanism for this acid-base
reaction and give the structures that would result from the
protonation of these products. Which phase (organic or aqueous)
would these protonated products be soluble in?
b) Which phase (organic or aqueous) would the
p-methylacetanilide be found in?
In step 5 of reaction 3, the reaction mixture containing the products shown below in ethyl acetate is extracted twice...
a) Which products (shown above) from reaction 3 can react with
HCl in an acid-base reaction? Show the mechanism for this acid-base
reaction and give the structures that would result from the
protonation of these products. Which phase (organic or aqueous)
would these protonated products be soluble in?
b) Which phase (organic or aqueous) would the
p-methylacetanilide be found in?
c) Why did we have to use hot ethanol for the
recrystallization?
d) Why did we have to cool the...
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