The molecular formula of compound A is C 6 H 12 . It reacts with one molar equivalent of H 2 /Pd. It reacts with OsO 4 to give the diol B. When oxidized with KMnO 4 , A gives propanoic acid and a ketone . The structures of A, B, C are to be given. All the reactions are to be written and explained. Concept introduction: From the molecular formula the degree of unsaturation can be calculated. The reaction with H 2 /Pd and that with OsO 4 shows the presence of double bonds. When oxidized with KMnO 4 a disubstituted carbon in a double bond is converted in to a ketone and a monosubstituted carbon in double bond gives a carboxylic acid . To give: The structures of compounds A, B and C which accounts for the reactions

Question

Propene undergoes a hydration reaction with water in the presence of an acid. a. There are two possible products for this reaction, both with the formula C3H8O. Show their structural formulas and names. b. Which of the two products do you predict will form. Explain

Answer 1

Question

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 8.SE, Problem 59AP

Interpretation Introduction

Interpretation:

The molecular formula of compound A is C₆H₁₂. It reacts with one molar equivalent of H₂/Pd. It reacts with OsO₄ to give the diol B. When oxidized with KMnO₄, A gives propanoic acid and a ketone. The structures of A, B, C are to be given. All the reactions are to be written and explained.

Concept introduction:

From the molecular formula the degree of unsaturation can be calculated. The reaction with H₂/Pd and that with OsO₄ shows the presence of double bonds. When oxidized with KMnO₄ a disubstituted carbon in a double bond is converted in to a ketone and a monosubstituted carbon in double bond gives a carboxylic acid.

To give:

The structures of compounds A, B and C which accounts for the reactions

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Propene undergoes a hydration reaction with water in the presence of an acid. a. There are two possible products for this reaction, both with the formula C3H8O. Show their structural formulas and names. b. Which of the two products do you predict will form. Explain

One mole of an unknown hydrocarbon, compound C, in the presence of a platinum catalyst, adds 98.9 L of hydrogen, measured at 744 mm Hg and 22 degrees C , to form a saturated alkane which contains one ring. When one mole of compound C is reacted with ozone, followed by reduction with (CH3)2S , four moles of only one product was formed, whose condensed molecular formula is CHO -CHO. Give the structure of compound C. Explain your reasoning

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Answer 2

Question

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 8.SE, Problem 59AP

Interpretation Introduction

Interpretation:

The molecular formula of compound A is C₆H₁₂. It reacts with one molar equivalent of H₂/Pd. It reacts with OsO₄ to give the diol B. When oxidized with KMnO₄, A gives propanoic acid and a ketone. The structures of A, B, C are to be given. All the reactions are to be written and explained.

Concept introduction:

From the molecular formula the degree of unsaturation can be calculated. The reaction with H₂/Pd and that with OsO₄ shows the presence of double bonds. When oxidized with KMnO₄ a disubstituted carbon in a double bond is converted in to a ketone and a monosubstituted carbon in double bond gives a carboxylic acid.

To give:

The structures of compounds A, B and C which accounts for the reactions

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 3

Question

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 8.SE, Problem 59AP

Interpretation Introduction

Interpretation:

The molecular formula of compound A is C₆H₁₂. It reacts with one molar equivalent of H₂/Pd. It reacts with OsO₄ to give the diol B. When oxidized with KMnO₄, A gives propanoic acid and a ketone. The structures of A, B, C are to be given. All the reactions are to be written and explained.

Concept introduction:

From the molecular formula the degree of unsaturation can be calculated. The reaction with H₂/Pd and that with OsO₄ shows the presence of double bonds. When oxidized with KMnO₄ a disubstituted carbon in a double bond is converted in to a ketone and a monosubstituted carbon in double bond gives a carboxylic acid.

To give:

The structures of compounds A, B and C which accounts for the reactions

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 4

Question

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 8.SE, Problem 59AP

Interpretation Introduction