What is Zaitsev’s rule? Give the mechanism for the acid-catalyzed E1 reaction of 2-butanol. Give the...
- What is Zaitsev’s rule?
- Give the mechanism for the acid-catalyzed E1 reaction of 2-butanol.
- Give the mechanism for the base-catalyzed E2 reaction of 2-bromobutane. Draw all possible products.
- You expect three products from the elimination reaction 2-butanol. What are they?
- The E2 mechanism is a one-step mechanism. True or False? Explain.
- Which of these two alcohols would you expect to be more reactive under H3PO4/aqueous conditions? Why? Give the structure of the main product in both cases.
1-phenyl-1-propanol
1 -cyclohexyl-1-propanol
- Give the structures for the alkenes produced by the dehydration of 2,3-dimethyl-2-butanol with concentrated H2SO4. Circle the major product.
- You are given a bottle of concentrated sulfuric acid (13 M). However, you need 1 M sulfuric acid, and nobody is present in the prep room to make it for you. How would you make 200 mL of the 1 M aqueous solution?
- You perform the reaction of 2 mL pinacolyl alcohol (3,3-dimethyl-2-butanol, d = 0.812 g/mL) with 5 mL of a mixture of concentrated phosphoric acid and concentrated sulfuric acid. You collect the product, and obtain 0.85 g. What is the product? Calculate the % yield.
Homework Answers
Add Answer to:
What is Zaitsev’s rule?
Give the mechanism for the acid-catalyzed E1 reaction of
2-butanol.
Give the...
2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol Show a mechanism for this reaction. 3. Acid-catalyzed hydration...
2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol Show a mechanism for this reaction. 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain. 4. Using 2-propanol as your only source of carbon, show how you would prepare 2-methyl- 2-pentanol
2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol. Show a mechanism for this reaction. 3. Acid-catalyzed hydration...
2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol. Show a mechanism for this reaction. 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain.
CHE 201 1. Give two reasons why concentrated sulfuric acid was added to the reaction 2....
CHE 201 1. Give two reasons why concentrated sulfuric acid was added to the reaction 2. In the synthesis of homohutano why was Synthesis of bromobutane why was the reaction mixture cooled in an ice bath before a concentrated sulfuric acid2 Describe what might happen if you forgot to cool the mixture. the esterification of butanol hu ur side products in the synthesis of hom feng butul hydrogen sulfate (A). This causes decreasing the yield of the desired product e...
Chemistry 2401 Experiment 7 Acid Catalyzed Dehydration of 3.3-Dimethyl-2-Butanol with Rearrangement Experiment 7 Pre-lab Assignment Dehydration...
Chemistry 2401 Experiment 7 Acid Catalyzed Dehydration of 3.3-Dimethyl-2-Butanol with Rearrangement Experiment 7 Pre-lab Assignment Dehydration of 3,3-Dimethyl-2-Butanol 1. Draw the structures of all the expected products from the following reactions: a) 3-methyl-3-pentanol + H = b)2-methylcyclohexanol + H - c) 2-methyl-2-butanol + H - d) 2,2-dimethylcyclohexanol + H = This reaction will give a complex mixture of products, since rearrangements can occur. Show the full mechanism for this reaction and how the possible products can form from the carbocation...
1. Give the complete reaction mechanism for the acid catalyzed hydration if 3,4-dimethyl-1-butene showing all inter...
1. Give the complete reaction mechanism for the acid catalyzed hydration if 3,4-dimethyl-1-butene showing all intermediates and products. (10 pts).
3. The esterification of butanol by sulfuric acid forms butyl hydrogen sulfate (A). This causes side...
3. The esterification of butanol by sulfuric acid forms butyl hydrogen sulfate (A). This causes side products in the synthesis of bromobutane decreasing the yield of the desired product. OH + H2So. - 0-5-OH + H2O A Ö Give the IUPAC name of two possible compounds of different functional groups that are products from this side reaction. Draw a mechanism for each starting from (A). 1) Side Product 1. IUPAC name is Draw Mechanism - 2) Side Product 2, different...
Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism. The first step is...
Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism. The first step is the protonation of the alcohol oxygen to form an oxonium ion Dehydration of 3-methyl-2-butanol forms one major and two minor organic products. Draw the structures, including hydrogen atoms, of the three organic products of this reaction :он H3 3 CH3 an oxonium ion 3-methyl-2-butanol Major Product Minor Product Minor Product
how does the mixture of isomeric alkenes produced by an acid-catalyzed dehydration reaction compare with the...
how does the mixture of isomeric alkenes produced by an
acid-catalyzed dehydration reaction compare with the alkene mixture
from a base-catalyzed dehydrochlorination reaction? Are either or
both sets or products influenced primarily by product
stability?
E1/E2 Elimination Reactions. Acid-Catalyzed Dehydration of 2-Me Base-Catalyzed Dehydrochlorination of 2-Chloro-2-methylbutane Acid-Catalyzed Dehydration of 2-Methyl-2-butanol and Adapted for an experiment published in More J.R - Hammond, C.N. Schatz, PF: Morrill, T.C.: Modern Projects and P. Hammond CN: Schatz, P.F., Morrill... Experiments in Organic Chemistry, 2nd...
Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism. The first step is...
Acid-catalyzed dehydration of secondary and tertiary alcohols
proceeds through an E1 mechanism. The first step is the protonation
of alcohol and oxygen to form an oxonium ion.
Dehydration of 3-methyl-2-butanol forms one major and two minor
organic products. Draw the structures, including hydrogen atoms, of
the three organic products of this reaction.
The 3.) is correct that is the minor product I came up with but
I cant get the answer correct for 1.) major product? and 2.) minor
product
Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism.
Acid-catalyzed dehydration of secondary and tertiary alcohols
proceeds through an E1 mechanism. The first step is the protonation
of the alcohol oxygen to form an oxonium ion. Dehydration of
3-methyl-2-butanol forms one major and two minor organic products.
Draw the structures, including hydrogen atoms, of the three organic
products of this reaction.
2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol Show a mechanism for this reaction. 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain. 4. Using 2-propanol as your only source of carbon, show how you would prepare 2-methyl- 2-pentanol
2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol. Show a mechanism for this reaction. 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain.
CHE 201 1. Give two reasons why concentrated sulfuric acid was added to the reaction 2. In the synthesis of homohutano why was Synthesis of bromobutane why was the reaction mixture cooled in an ice bath before a concentrated sulfuric acid2 Describe what might happen if you forgot to cool the mixture. the esterification of butanol hu ur side products in the synthesis of hom feng butul hydrogen sulfate (A). This causes decreasing the yield of the desired product e...
Chemistry 2401 Experiment 7 Acid Catalyzed Dehydration of 3.3-Dimethyl-2-Butanol with Rearrangement Experiment 7 Pre-lab Assignment Dehydration of 3,3-Dimethyl-2-Butanol 1. Draw the structures of all the expected products from the following reactions: a) 3-methyl-3-pentanol + H = b)2-methylcyclohexanol + H - c) 2-methyl-2-butanol + H - d) 2,2-dimethylcyclohexanol + H = This reaction will give a complex mixture of products, since rearrangements can occur. Show the full mechanism for this reaction and how the possible products can form from the carbocation...
1. Give the complete reaction mechanism for the acid catalyzed hydration if 3,4-dimethyl-1-butene showing all intermediates and products. (10 pts).
3. The esterification of butanol by sulfuric acid forms butyl hydrogen sulfate (A). This causes side products in the synthesis of bromobutane decreasing the yield of the desired product. OH + H2So. - 0-5-OH + H2O A Ö Give the IUPAC name of two possible compounds of different functional groups that are products from this side reaction. Draw a mechanism for each starting from (A). 1) Side Product 1. IUPAC name is Draw Mechanism - 2) Side Product 2, different...
Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism. The first step is the protonation of the alcohol oxygen to form an oxonium ion Dehydration of 3-methyl-2-butanol forms one major and two minor organic products. Draw the structures, including hydrogen atoms, of the three organic products of this reaction :он H3 3 CH3 an oxonium ion 3-methyl-2-butanol Major Product Minor Product Minor Product
how does the mixture of isomeric alkenes produced by an
acid-catalyzed dehydration reaction compare with the alkene mixture
from a base-catalyzed dehydrochlorination reaction? Are either or
both sets or products influenced primarily by product
stability?
E1/E2 Elimination Reactions. Acid-Catalyzed Dehydration of 2-Me Base-Catalyzed Dehydrochlorination of 2-Chloro-2-methylbutane Acid-Catalyzed Dehydration of 2-Methyl-2-butanol and Adapted for an experiment published in More J.R - Hammond, C.N. Schatz, PF: Morrill, T.C.: Modern Projects and P. Hammond CN: Schatz, P.F., Morrill... Experiments in Organic Chemistry, 2nd...
Acid-catalyzed dehydration of secondary and tertiary alcohols
proceeds through an E1 mechanism. The first step is the protonation
of alcohol and oxygen to form an oxonium ion.
Dehydration of 3-methyl-2-butanol forms one major and two minor
organic products. Draw the structures, including hydrogen atoms, of
the three organic products of this reaction.
The 3.) is correct that is the minor product I came up with but
I cant get the answer correct for 1.) major product? and 2.) minor
product
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