Hydrocarbon A (C 9 H 12 ) absorbs 3 equivalents of H 2 in the presence of Pd/C to yield B (C 9 H 18 ). A when treated with aqueous H 2 SO 4 in the presence of Hg(II) gives two isomeric ketones C and D . A upon oxidation with KMnO 4 gives a mixture of acetic acid and tricarboxylic acid E . Based on these data, structures for the compounds A - D are to be given and the reactions are to be written. Concept introduction: The degree of unsaturation can be calculated by comparing the molecular formula of compound given with that of its parent hydrocarbon. Both alkenes and alkynes yield alkanes by adsorbing H 2 in the presence of Pd catalyst. Alkynes require two equivalents of H 2 while alkenes require one equivalent of H 2 to give alkanes. Internal alkynes will yield a mixture of isomeric ketones when treated with aqueous H 2 SO 4 in the presence of mercury (II) if they are symmetrically substituted. When oxidized with KMnO 4 , monosubstituted carbons in both double and triple bonds get oxidized to carboxylic acids. To give: Based on the data given, the structures of A - D and to write the reactions.

Question

Predict the major products of the following organic reaction: Some important notes: Δ CN ? • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. ONO reaction. Click and drag to start drawing a structure.

Answer 1

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Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 9.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Hydrocarbon A(C₉H₁₂) absorbs 3 equivalents of H₂ in the presence of Pd/C to yield B(C₉H₁₈). A when treated with aqueous H₂SO₄ in the presence of Hg(II) gives two isomeric ketones C and D. A upon oxidation with KMnO₄ gives a mixture of acetic acid and tricarboxylic acid E. Based on these data, structures for the compounds A-D are to be given and the reactions are to be written.

Concept introduction:

The degree of unsaturation can be calculated by comparing the molecular formula of compound given with that of its parent hydrocarbon. Both alkenes and alkynes yield alkanes by adsorbing H₂ in the presence of Pd catalyst. Alkynes require two equivalents of H₂ while alkenes require one equivalent of H₂ to give alkanes. Internal alkynes will yield a mixture of isomeric ketones when treated with aqueous H₂SO₄ in the presence of mercury (II) if they are symmetrically substituted. When oxidized with KMnO₄, monosubstituted carbons in both double and triple bonds get oxidized to carboxylic acids.

To give:

Based on the data given, the structures of A-D and to write the reactions.

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Predict the major products of the following organic reaction: Some important notes: Δ CN ? • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. ONO reaction. Click and drag to start drawing a structure.

The following product was made from diethyl ketone and what other reagent(s)? £ HO 10 2-pentyne 1-butyne and NaNH2 ☐ 1-propanol ☐ pyridine butanal ☐ pentanoate

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Answer 2

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100%

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 9.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Hydrocarbon A(C₉H₁₂) absorbs 3 equivalents of H₂ in the presence of Pd/C to yield B(C₉H₁₈). A when treated with aqueous H₂SO₄ in the presence of Hg(II) gives two isomeric ketones C and D. A upon oxidation with KMnO₄ gives a mixture of acetic acid and tricarboxylic acid E. Based on these data, structures for the compounds A-D are to be given and the reactions are to be written.

Concept introduction:

The degree of unsaturation can be calculated by comparing the molecular formula of compound given with that of its parent hydrocarbon. Both alkenes and alkynes yield alkanes by adsorbing H₂ in the presence of Pd catalyst. Alkynes require two equivalents of H₂ while alkenes require one equivalent of H₂ to give alkanes. Internal alkynes will yield a mixture of isomeric ketones when treated with aqueous H₂SO₄ in the presence of mercury (II) if they are symmetrically substituted. When oxidized with KMnO₄, monosubstituted carbons in both double and triple bonds get oxidized to carboxylic acids.

To give:

Based on the data given, the structures of A-D and to write the reactions.

Expert Solution & Answer

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See solution

Check out sample textbook solution

Answer 3

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Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 9.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Hydrocarbon A(C₉H₁₂) absorbs 3 equivalents of H₂ in the presence of Pd/C to yield B(C₉H₁₈). A when treated with aqueous H₂SO₄ in the presence of Hg(II) gives two isomeric ketones C and D. A upon oxidation with KMnO₄ gives a mixture of acetic acid and tricarboxylic acid E. Based on these data, structures for the compounds A-D are to be given and the reactions are to be written.

Concept introduction:

The degree of unsaturation can be calculated by comparing the molecular formula of compound given with that of its parent hydrocarbon. Both alkenes and alkynes yield alkanes by adsorbing H₂ in the presence of Pd catalyst. Alkynes require two equivalents of H₂ while alkenes require one equivalent of H₂ to give alkanes. Internal alkynes will yield a mixture of isomeric ketones when treated with aqueous H₂SO₄ in the presence of mercury (II) if they are symmetrically substituted. When oxidized with KMnO₄, monosubstituted carbons in both double and triple bonds get oxidized to carboxylic acids.

To give:

Based on the data given, the structures of A-D and to write the reactions.

Expert Solution & Answer

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See solution

Check out sample textbook solution

Answer 4

Question

100%

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 9.SE, Problem 54AP

Interpretation Introduction