Reaction Types & Reagents

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These flashcards cover key reagents, reaction types, and products associated with organic chemistry reaction mechanisms.

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15 Terms

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Reduction Reactions

Reactions that involve the gain of electrons or a decrease in oxidation state, often resulting in the formation of alcohols from carbonyl compounds.

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NaBH4

A reducing agent used for the reduction of aldehydes and ketones to primary or secondary alcohols.

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LiAlH4

A more powerful reducing agent than NaBH4, capable of reducing aldehydes, ketones, esters, and carboxylic acids to alcohols.

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H₂ / Pd or Pt

A catalytic hydrogenation method used to convert alkenes, alkynes, and ketones to alkanes or alcohols.

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Oxidation Reactions

Reactions that involve the loss of electrons or an increase in oxidation state, typically converting alcohols to carbonyls or carboxylic acids.

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PCC

Pyridinium chlorochromate, a mild oxidizing agent used to convert primary alcohols to aldehydes without further oxidation.

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Jones reagent

A strong oxidizing reagent (CrO3/H2SO4) used for converting primary alcohols to carboxylic acids and secondary alcohols to ketones.

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KMnO4 (cold, dilute)

A reagent used for the oxidation of alkenes to vicinal diols.

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Halogenation

A reaction involving the addition of halogen (Br2 or Cl2) across a double bond to form vicinal dihalides.

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Hydroboration-oxidation

A two-step reaction process that converts alkenes to alcohols, where the addition of B2H6 followed by oxidation results in anti-Markovnikov addition.

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Nucleophilic Addition to Carbonyls

Reactions where nucleophiles attack the electrophilic carbon in carbonyl compounds.

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Grignard (RMgX)

A powerful nucleophile used in the addition to carbonyl compounds to form alcohols after acid workup.

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Cleavage Reactions

Reactions that involve breaking double bonds (alkenes) to form smaller carbonyl compounds (aldehydes or ketones).

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Friedel-Crafts alkylation

A type of substitution reaction that introduces an alkyl group onto an aromatic ring using an alkyl halide and a Lewis acid catalyst.

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Friedel-Crafts acylation

A substitution reaction that introduces an acyl group onto an aromatic ring, using an acyl chloride and a Lewis acid.