CHM243 Reactions TT1

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Last updated 12:22 AM on 2/2/26
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25 Terms

1
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<p>What’s the product</p>

What’s the product

Bromination reaction

<p>Bromination reaction </p>
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<p>Product? </p>

Product?

Chlorination reaction

<p>Chlorination reaction </p>
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<p>Product? </p>

Product?

Iodination reaction

<p>Iodination reaction </p>
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<p>Product? </p>

Product?

Fluorination reaction

<p>Fluorination reaction </p>
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<p>Product? </p>

Product?

Aromatic nitration reaction

<p>Aromatic nitration reaction </p>
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<p>Product? </p>

Product?

Aromatic sulfonation reaction

<p>Aromatic sulfonation reaction </p>
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<p>Product? </p>

Product?

Friedel Crafts Alkylation Reaction

<p>Friedel Crafts Alkylation Reaction </p>
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<p>Product? </p>

Product?

Friedel Crafts Acylation Reaction

<p>Friedel Crafts Acylation Reaction </p>
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<p>Product? </p>

Product?

It’s also a friedel crafts reaction

<p>It’s also a friedel crafts reaction </p>
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<p>Product? </p>

Product?

Oxidation of Aldehydes

<p>Oxidation of Aldehydes </p>
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<p>Product? </p>

Product?

Nucleophilic addition of water: hydration

<p>Nucleophilic addition of water: hydration </p>
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<p>Product? </p>

Product?

Nucleophilic addition of water: hydration

<p>Nucleophilic addition of water: hydration </p>
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<p>Product?</p>

Product?

Cyanohydrin formation: nucleophilic addn reaction

<p>Cyanohydrin formation: nucleophilic addn reaction </p>
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<p>Product? </p>

Product?

Reduction reaction: nucleophilic addition of HCN (cyanohydride formation)

<p>Reduction reaction: nucleophilic addition of HCN (cyanohydride formation) </p>
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<p>Product? </p>

Product?

Hot acid catalysis: nucleophilic addition of HCN (cyanohydride formation)

<p>Hot acid catalysis: nucleophilic addition of HCN (cyanohydride formation) </p>
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<p>Product</p>

Product

Alcohol formation: Nucleophilic addition of hydride reagent

<p>Alcohol formation: Nucleophilic addition of hydride reagent </p>
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<p>Product</p>

Product

Alcohol formation: Nucleophilic addition of Hydride reagent

<p>Alcohol formation: Nucleophilic addition of Hydride reagent </p>
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<p>Product? </p>

Product?

Nucleophilic addition of Grignard reagent

<p>Nucleophilic addition of Grignard reagent </p>
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<p>Product? </p>

Product?

Nucleophilic addition of Grignard reagent

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<p>Product? </p>

Product?

Nucleophilic addition of amine: imine formation

<p>Nucleophilic addition of amine: imine formation </p>
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<p>Product? </p>

Product?

Nucleophilic addition of amine: enamine formation

<p>Nucleophilic addition of amine: enamine formation </p>
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<p>Product? </p>

Product?

Nucleophilic addition of hydrazine: wolff kishner reaction

<p>Nucleophilic addition of hydrazine: wolff kishner reaction </p>
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<p>Product? </p>

Product?

Nucleophilic addition of alcohols: acetal formation

<p>Nucleophilic addition of alcohols: acetal formation </p>
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<p>Product? </p>

Product?

Nucleophilic addition of alcohols: acetal formation

<p>Nucleophilic addition of alcohols: acetal formation </p>
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<p>Product? </p>

Product?

Wittig reaction
Good for turning aldehydes and ketones into alkenes

<p>Wittig reaction<br>Good for turning aldehydes and ketones into alkenes </p>