Section: Module 8: Lesson 2: Synthesis of Alcohols | Organic Chemistry 1 | NextGenU.org

  • Student Learning Outcomes:
    Upon completion of this lesson, you will be able to:
    • Examine the methods used to synthesize alcohols through substitution reactions.
    • Break down the reaction mechanisms for the reduction of an aldehyde or ketone using sodium borohydride or lithium aluminum hydride.
    • Appraise the reduction of carboxylic acids and esters using lithium aluminum hydride.
    • Explain the reaction mechanisms and products for the Grignard synthesis of alcohols from carbonyl compounds.
    • Deduce the product formed from the reaction of an ester with a given Grignard reagent.
    Approximate time required for the readings for this lesson (at 144 words/minute): 1 hour and 3 minutes.

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    • Required Learning Resources and Activities
    • Read the entire section. (4 minutes)

      Chemistry libre texts 

    • Read the entire webpage. (8 minutes)

      Chemistry libre texts - 2021

    • Read the entire webpage. (9 minutes)

      Chemistry libre texts - 2021