13. Alcohols and Carbonyl Compounds
Reducing Agent
13. Alcohols and Carbonyl Compounds
Reducing Agent - Video Tutorials & Practice Problems
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Reducing Agents
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ProblemWhat is the product of the reaction?
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D
No reaction
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ProblemWhat is the product of the reacion?
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B
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No reaction
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ProblemWhat is the product of the reaction?
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B
C
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No reaction
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PRACTICE PROBLEMS AND ACTIVITIES (45)
- Predict the products you would expect from the reaction of LiALH4 follwoed by hydrolysis with the following co...
- Predict the products you would expect from the reaction of LiALH4 follwoed by hydrolysis with the following co...
- Predict the products you would expect from the reaction of NaBH4 with the following compounds. You may assume ...
- Predict the products you would expect from the reaction of NaBH4 with the following compounds. You may assume ...
- Suggest carbonyl compounds and reducing agents that might be used to form the following alcohols (b) 1-cyclohe...
- Suggest carbonyl compounds and reducing agents that might be used to form the following alcohols (a) octan-1-o...
- Show how you would accomplish the following transformations. You may use any additional reagents you need. (d)...
- Show how you would accomplish the following transformations. You may use any additional reagents you need. (c)...
- Compounds containing deuterium (D = 2 H) are useful for kinetic studies and metabolic studies with new pharmac...
- Show how you would synthesize the following alcohol by reducing appropriate carbonyl compound. (c) 2-methylhe...
- Show how you would synthesize the following alcohol by reducing appropriate carbonyl compound. (a) heptan-1-o...
- Describe how each of the following compounds could be synthesized from the given starting material. a.
- Write the appropriate reagent over each arrow.
- Predict the products of the following reactions. (c) 1-methylcyclohexanol + H2SO4, heat (d) product of (c) + H...
- Develop syntheses for the following compounds. As starting materials, you may use cyclopentanol, alcohols co...
- Develop syntheses for the following compounds. As starting materials, you may use cyclopentanol, alcohols co...
- Suggest the most appropriate method for each of the following laboratory syntheses. In each case, suggest bot...
- Identify the alcohols that would undergo oxidation to produce the following carbonyl compounds. (d)
- Propose a synthesis of the carbonyl(s) using the (ii) dihydroxylation/periodic acid cleavage pathways. (a)
- Propose a synthesis of the carbonyl(s) using the (ii) dihydroxylation/periodic acid cleavage pathways. (b)
- Give the structures of the products represented by letters in this synthesis. Part 2:
- a. Show the reagents required to form the primary alcohol in each of the following reactions.
- a. Show the reagents required to form the primary alcohol in each of the following reactions.
- a. Show the reagents required to form the primary alcohol in each of the following reactions.
- a. Show the reagents required to form the primary alcohol in each of the following reactions.
- a. What would have been the product of the preceding reaction with LiAlH4 if the keto group had not been prote...
- Identify A through O:
- b. What reagent could you use to reduce only the keto group?
- How would you make the following compounds from N-benzylbenzamide? c. benzyl alcohol
- How would you make the following compounds from N-benzylbenzamide? a. dibenzylamine
- How could you convert N-methylbenzamide to the following compounds? a. N-methylbenzylamine
- Predict the major products of the following reactions. (f) < of reaction>
- Show how you would accomplish the following syntheses. You may use whatever additional reagents you need. (a)...
- Sodium triacetoxyborohydride, NaBH(OAc)3, is a mild reducing agent that reduces aldehydes much more quickly ...
- Show how you would accomplish the following synthetic conversions. You may use any additional reagents and s...
- An ether extraction of nutmeg gives large quantities of trimyristin, a waxy crystalline solid of melting point...
- Show how you would accomplish the following synthetic transformations. You may use any necessary reagents. (a...
- The esters shown differ only by the alkoxy group. (i) Predict the product(s) obtained when these react with DI...
- Predict the product of the following reductions.(a) <IMAGE>
- Predict the product of the following reductions.(d) <IMAGE>
- Show a mechanism for the lithium aluminum hydride reduction of benzoic anhydride.<IMAGE>
- Predict the product of the following reaction sequences.(a) <IMAGE>
- Predict the product of the following reductions.(b) <IMAGE>
- Predict the product of the following reductions.(c) <IMAGE>
- How would you reduce the alkene in the presence of a carboxylic acid?