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9.6: Synthesis of Alcohols: Oxidation-Reduction Relation Between Alcohols and Carbonyl Compounds

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    201173
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    Objectives

    After completing this section, you should be able to

    1. determine whether a given reaction should be classified as an oxidation or a reduction.
    2. write an equation to represent the reduction of an aldehyde or ketone using sodium borohydride or lithium aluminum hydride.
      1. discuss the relative advantages and disadvantages of using sodium borohydride or lithium aluminum hydride to reduce aldehydes or ketones to alcohols.
      2. identify the product formed from the reduction of a given aldehyde or ketone.
      3. identify the aldehyde or ketone that should be used to produce a given alcohol in a reduction reaction.
      4. identify the best reagent to carry out the reduction of a given aldehyde or ketone.
    3. write an equation to represent the reduction of an ester or a carboxylic acid to an alcohol.
      1. identify the product formed from the reduction of a given ester or carboxylic acid.
      2. identify the esters or carboxylic acids that could be reduced to form a given alcohol.
    Key Terms

    Make certain that you can define, and use in context, the key terms below.

    • (organic) oxidation
    • (organic) reduction
    Study Notes

    In your course in first‑year general chemistry, you probably discussed oxidation‑reduction reactions in terms of the transfer of electrons and changes in oxidation numbers (oxidation states). In organic chemistry, it is often more convenient to regard reduction as the gain of hydrogen or loss of oxygen, and oxidation as the gain of oxygen or the loss of hydrogen. There is no contradiction in using these various definitions. For example, when hydrogen is added across the double bond of ethene to reduce it to ethane, the oxidation number of the doubly bonded carbon atoms decreases from −II to −III. Similarly, when 2‑propanol

    is oxidized to acetone

    hydrogen is removed from the compound and the oxidation number of the central carbon atom increases from 0 to +II. If necessary, review the concept of oxidation number.

    Reduction of Aldehydes and Ketones

    The most common sources of the hydride Nucleophile are lithium aluminum hydride (LiAlH4) and sodium borohydride (NaBH4). Note! The hydride anion is not present during this reaction; rather, these reagents serve as a source of hydride due to the presence of a polar metal-hydrogen bond. Because aluminum is less electronegative than boron, the Al-H bond in LiAlH4 is more polar, thereby, making LiAlH4 a stronger reducing agent.

    Diagram showing sodium borohydride, lithium aluminum hydride, and a hydride nucleophile. Sodium and lithium hold positive charges, while boron, aluminum, and the hydride nucleophile hold negative charges.

    Addition of a hydride anion (H:-) to an aldehyde or ketone gives an alkoxide anion, which on protonation yields the corresponding alcohol. Aldehydes produce 1º-alcohols and ketones produce 2º-alcohols.

    In metal hydrides reductions the resulting alkoxide salts are insoluble and need to be hydrolyzed (with care) before the alcohol product can be isolated. In the sodium borohydride reduction the methanol solvent system achieves this hydrolysis automatically. In the lithium aluminum hydride reduction water is usually added in a second step. The lithium, sodium, boron and aluminum end up as soluble inorganic salts at the end of either reaction. Note! LiAlH4 and NaBH4 are both capable of reducing aldehydes and ketones to the corresponding alcohol.

    Example 17.4.1

    Benzaldehyde reacts with sodium borohydride in methanol to form benzyl alcohol.

    Mechanism

    This mechanism is for a LiAlH4 reduction. The mechanism for a NaBH4 reduction is the same except methanol is the proton source used in the second step.

    1) Nucleopilic attack by the hydride anion

    2) The alkoxide is protonated

    Biological Reduction

    Addition to a carbonyl by a semi-anionic hydride, such as NaBH4, results in conversion of the carbonyl compound to an alcohol. The hydride from the BH4- anion acts as a nucleophile, adding H- to the carbonyl carbon. A proton source can then protonate the oxygen of the resulting alkoxide ion, forming an alcohol.

    17-4-Equation.png

    Formally, that process is referred to as a reduction. Reduction generally means a reaction in which electrons are added to a compound; the compound that gains electrons is said to be reduced. Because hydride can be thought of as a proton plus two electrons, we can think of conversion of a ketone or an aldehyde to an alcohol as a two-electron reduction. An aldehyde plus two electrons and two protons becomes an alcohol.

    Aldehydes, ketones and alcohols are very common features in biological molecules. Converting between these compounds is a frequent event in many biological pathways. However, semi-anionic compounds like sodium borohydride don't exist in the cell. Instead, a number of biological hydride donors play a similar role.

    NADH is a common biological reducing agent. NADH is an acronym for nicotinamide adenine dinucleotide hydride. Insetad of an anionic donor that provides a hydride to a carbonyl, NADH is actually a neutral donor. It supplies a hydride to the carbonyl under very specific circumstances. In doing so, it forms a cation, NAD+. However, NAD+ is stabilized by the fact that its nicotinamide ring is aromatic; it was not aromatic in NADH.

    17-4-NADH.png

    Reduction of Carboxylic Acids and Esters

    Carboxylic acids can be converted to 1o alcohols using Lithium aluminum hydride (LiAlH4). Note that NaBH4 is not strong enough to convert carboxylic acids or esters to alcohols. An aldehyde is produced as an intermediate during this reaction, but it cannot be isolated because it is more reactive than the original carboxylic acid.

    Esters can be converted to 1o alcohols using LiAlH4, while sodium borohydride (\(NaBH_4\)) is not a strong enough reducing agent to perform this reaction.

     

    Example 17.4.2

    Example Hydride Reduction CA.png

    Example Hydride Reduction Ester.png

    Worked Example 17.4.1

    How would you prepare the following molecules using a hydride reduction?

    a)

    Worked Example Questions.png

    b)

    Worked Example QuestionsB.png

    Answer

    Analysis: The first step is to note if the target molecule is a 1o or 2o alcohol. Primary alcohols can be made by the hydride reduction of an aldehyde, carboxylic acid, or ester while secondary alcohols are made by the reduction of ketones. A 3o alcohol cannot be made by a hydride reduction. Also, it is important to remember than aldehydes and ketones can be reduced by both NaBH4 and LiAlH4 whereas carboxylic acids and ester can only be reduced by LiAlH4.

    a) Because the target molecule is a secondary alcohol the starting material must be a ketone.

    Worked Example Answer a.png

    b) Because the target molecule is a primary alcohol the starting material could be an aldehyde, a carboxylic acid, or an ester.

    Worked Example Questions b.png

    Exercises

    Exercise 17.4.1

    Give the aldehyde, ketone, or carboxylic acid (there can be multiple answers) that could be reduced to form the following alcohols.

    17_4_1.svg

    Answer

    17_4_1_Answer.svg

    Exercise 17.4.2

    Given the following alcohol, draw the structure from which it could be derived using only NaBH4.

    17_4_2.svg

    Answer

    Note: NaBH4 is only a strong enough reducing agent to reduce ketones and aldehydes.

    17_4_2_Answer.svg


    9.6: Synthesis of Alcohols: Oxidation-Reduction Relation Between Alcohols and Carbonyl Compounds is shared under a not declared license and was authored, remixed, and/or curated by LibreTexts.