Ch19. Aldehydes and Ketones: Nucleophilic Addition Reactions Nucleophilic Addition Reaction Aldehydes and ketones are reduced to yield 1° and 2° alcohols, respectively - Reduction (hydride attack: H): NaBH, or LIAIH, (stronger) _H 1) NaBH4 2) HⓇ - Grignard reagents (R-MgX) give alcohols MgBr 1) + - Addition of HCN yields cyanohydrins, RCH(OH)CEN NaCN 2) H₂O* HCN
Ch19. Aldehydes and Ketones: Nucleophilic Addition Reactions Nucleophilic Addition Reaction Aldehydes and ketones are reduced to yield 1° and 2° alcohols, respectively - Reduction (hydride attack: H): NaBH, or LIAIH, (stronger) _H 1) NaBH4 2) HⓇ - Grignard reagents (R-MgX) give alcohols MgBr 1) + - Addition of HCN yields cyanohydrins, RCH(OH)CEN NaCN 2) H₂O* HCN
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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- Reduction of aldehyde with NaBH4
- Reaction of aldehyde with Grignard reagent
- Addition of HCN to ketone
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