All Chapters
Ch. 1 - A Review of General Chemistry	4hrs & 47mins	0% complete	Worksheet Start
Ch. 2 - Molecular Representations	1hr & 12mins	0% complete	Worksheet Start
Ch. 3 - Acids and Bases	2hrs & 45mins	0% complete	Worksheet Start
Ch. 4 - Alkanes and Cycloalkanes	4hrs & 18mins	0% complete	Worksheet Start
Ch. 5 - Chirality	3hrs & 33mins	0% complete	Worksheet Start
Ch. 6 - Thermodynamics and Kinetics	1hr & 19mins	0% complete	Worksheet Start
Ch. 7 - Substitution Reactions	1hr & 46mins	0% complete	Worksheet Start
Ch. 8 - Elimination Reactions	2hrs & 24mins	0% complete	Worksheet Start
Ch. 9 - Alkenes and Alkynes	2hrs & 10mins	0% complete	Worksheet Start
Ch. 10 - Addition Reactions	3hrs & 33mins	0% complete	Worksheet Start
Ch. 11 - Radical Reactions	1hr & 57mins	0% complete	Worksheet Start
Ch. 12 - Alcohols, Ethers, Epoxides and Thiols	2hrs & 34mins	0% complete	Worksheet Start
Ch. 13 - Alcohols and Carbonyl Compounds	2hrs & 14mins	0% complete	Worksheet Start
Ch. 14 - Synthetic Techniques	1hr & 28mins	0% complete	Worksheet Start
Ch. 15 - Analytical Techniques: IR, NMR, Mass Spect	7hrs & 18mins	0% complete	Worksheet Start
Ch. 16 - Conjugated Systems	5hrs & 49mins	0% complete	Worksheet Start
Ch. 17 - Aromaticity	2hrs & 24mins	0% complete	Worksheet Start
Ch. 18 - Reactions of Aromatics: EAS and Beyond	4hrs & 31mins	0% complete	Worksheet Start
Ch. 19 - Aldehydes and Ketones: Nucleophilic Addition	4hrs & 54mins	0% complete	Worksheet Start
Ch. 20 - Carboxylic Acid Derivatives: NAS	2hrs & 3mins	0% complete	Worksheet Start
Ch. 21 - Enolate Chemistry: Reactions at the Alpha-Carbon	1hr & 59mins	0% complete	Worksheet Start
Ch. 22 - Condensation Chemistry	2hrs & 13mins	0% complete	Worksheet Start
Ch. 23 - Amines	1hr & 43mins	0% complete	Worksheet Start
Ch. 24 - Carbohydrates	5hrs & 56mins	0% complete	Worksheet Start
Ch. 25 - Phenols	15mins	0% complete	Worksheet Start
Ch. 26 - Amino Acids, Peptides, and Proteins	2hrs & 54mins	0% complete	Worksheet Start

Cyanohydrin

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Sections
Naming Aldehydes	8 mins	0 completed	Learn
Naming Ketones	8 mins	0 completed	Learn
Oxidizing and Reducing Agents	9 mins	0 completed	Learn
Oxidation of Alcohols	40 mins	0 completed	Learn
Ozonolysis	8 mins	0 completed	Learn
DIBAL	6 mins	0 completed	Learn
Alkyne Hydration	9 mins	0 completed	Learn
Nucleophilic Addition	8 mins	0 completed	Learn
Cyanohydrin	11 mins	0 completed	Learn Summary
Organometallics on Ketones	18 mins	0 completed	Learn
Overview of Nucleophilic Addition of Solvents	13 mins	0 completed	Learn
Hydrates	6 mins	0 completed	Learn
Hemiacetal	10 mins	0 completed	Learn Summary
Acetal	12 mins	0 completed	Learn Summary
Acetal Protecting Group	16 mins	0 completed	Learn Summary
Thioacetal	7 mins	0 completed	Learn Summary
Imine vs Enamine	15 mins	0 completed	Learn Summary
Addition of Amine Derivatives	5 mins	0 completed	Learn Summary
Wolff Kishner Reduction	7 mins	0 completed	Learn Summary
Baeyer-Villiger Oxidation	28 mins	0 completed	Learn Summary
Acid Chloride to Ketone	7 mins	0 completed	Learn
Nitrile to Ketone	9 mins	0 completed	Learn Summary
Wittig Reaction	19 mins	0 completed	Learn Summary
Ketone and Aldehyde Synthesis Reactions	14 mins	0 completed	Learn

Additional Practice
Physical Properties of Ketones and Aldehydes
Multi-Functionalized Carbonyl Nomenclauture
Catalytic Reduction of Carbonyls
Tollens’s Test
Fehling’s Test
Alkyne Hydroboration to Yield Aldehydes
Nucleophilic Addition Reactivity
Strecker Synthesis
Synthesis Involving Acetals
Reduction of Carbonyls to Alkanes
Clemmensen vs Wolff-Kischner
Baeyer-Villiger Oxidation Synthesis
Weinreb Ketone Synthesis
Wittig Retrosynthesis
Horner–Wadsworth–Emmons Reaction
Carbonyl Missing Reagent
Carbonyl Hydrolysis
Carbonyl Synthesis
Carbonyl Retrosynthesis
Reactions of Ketenes
Ketene Synthesis

Additional Guides
Acetal and Hemiacetal

Learn Additional Practice Summary

Next SectionOrganometallics on Ketones

Solution: Based on the principles of acidic and basic cleavage as well epoxidation determine the necessary reagents for the each of the following transformations.

Name: Based on the principles of acidic and basic cleavage as well epoxidation determine the necessary reagents for the each of the following transformations.
Uploaded: 2017-03-07T12:28:26.000-05:00
Duration: 2 min 9 s
Description: Watch the video solution for the question: Based on the principles of acidic and basic cleavage as well epoxidation determine the necessary reagents for the each of the following transformations.

Problem

Based on the principles of acidic and basic cleavage as well epoxidation determine the necessary reagents for the each of the following transformations.

Cyanohydrin

Solution: Based on the principles of acidic and basic cleavage as well epoxidation determine the necessary reagents for the each of the following transformations.

Problem

Practice Problems

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