The equation for the given crossed Claisen condensation has to be completed. Concept introduction: When two molecules of an ester undergo condensation is called claisen condensation. Like in aldol reaction, in claisen condensation one molecule is a nucleophile and the other molecule is an electrophile. A claisen condensation reaction is a reversible reaction and occurs in the presence of a strong base. The first step of claisen condensation is the removal of a proton from alpha carbon by a base and then the addition of enolate ion formed to the second ester molecule forming a β-ketoester. A crossed-claisen condensation is also a condensation reaction between a ketone and an ester. Primarily one product will form from crossed-claisen condensation when one of the ketone or easter do not have any alpha hydrogens.

Question

Draw the structure of A, the minor E1 product of the reaction. Cl Skip Part Check F1 esc CH_CH OH, D 3 2 Click and drag to start drawing a structure. 80 R3 F4 F2 F3 @ 2 # $ 4 3 Q W 95 % KO 5 F6 A F7 × G ☐ Save For Later Sub 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy C ►II A A F8 F9 F10 FL 6 7 88 & * 8 9 LLI E R T Y U A S D lock LL F G H 0 P J K L Z X C V B N M 9 H

Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 19.3, Problem 19.5P

Interpretation Introduction

Interpretation:

The equation for the given crossed Claisen condensation has to be completed.

Concept introduction: When two molecules of an ester undergo condensation is called claisen condensation. Like in aldol reaction, in claisen condensation one molecule is a nucleophile and the other molecule is an electrophile.

A claisen condensation reaction is a reversible reaction and occurs in the presence of a strong base.

The first step of claisen condensation is the removal of a proton from alpha carbon by a base and then the addition of enolate ion formed to the second ester molecule forming a β-ketoester.

A crossed-claisen condensation is also a condensation reaction between a ketone and an ester. Primarily one product will form from crossed-claisen condensation when one of the ketone or easter do not have any alpha hydrogens.

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Draw the structure of A, the minor E1 product of the reaction. Cl Skip Part Check F1 esc CH_CH OH, D 3 2 Click and drag to start drawing a structure. 80 R3 F4 F2 F3 @ 2 # $ 4 3 Q W 95 % KO 5 F6 A F7 × G ☐ Save For Later Sub 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy C ►II A A F8 F9 F10 FL 6 7 88 & * 8 9 LLI E R T Y U A S D lock LL F G H 0 P J K L Z X C V B N M 9 H

From the choices given, which two substances have the same crystal structure? (Select both) Group of answer choices ZnS (zincblende) Diamond TiO2 (rutile) ZnS (wurtzite)

Potassium (K) blends with germanium (Ge) to form a Zintl phase with a chemical formula of K4Ge4. Which of the following elements would you expect potassium to blend with to form an alloy? Electronegativities: As (2.0), Cl (3.0), Ge (1.8), K (0.8), S (2.5), Ti (1.5) Group of answer choices Arsenic (As) Sulfur (S) Chlorine (Cl) Titanium (Ti)

Answer 2

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Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 19.3, Problem 19.5P

Interpretation Introduction

Interpretation:

The equation for the given crossed Claisen condensation has to be completed.

Concept introduction: When two molecules of an ester undergo condensation is called claisen condensation. Like in aldol reaction, in claisen condensation one molecule is a nucleophile and the other molecule is an electrophile.

A claisen condensation reaction is a reversible reaction and occurs in the presence of a strong base.

The first step of claisen condensation is the removal of a proton from alpha carbon by a base and then the addition of enolate ion formed to the second ester molecule forming a β-ketoester.

A crossed-claisen condensation is also a condensation reaction between a ketone and an ester. Primarily one product will form from crossed-claisen condensation when one of the ketone or easter do not have any alpha hydrogens.

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Answer 3

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Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 19.3, Problem 19.5P

Interpretation Introduction

Interpretation:

The equation for the given crossed Claisen condensation has to be completed.

Concept introduction: When two molecules of an ester undergo condensation is called claisen condensation. Like in aldol reaction, in claisen condensation one molecule is a nucleophile and the other molecule is an electrophile.

A claisen condensation reaction is a reversible reaction and occurs in the presence of a strong base.

The first step of claisen condensation is the removal of a proton from alpha carbon by a base and then the addition of enolate ion formed to the second ester molecule forming a β-ketoester.

A crossed-claisen condensation is also a condensation reaction between a ketone and an ester. Primarily one product will form from crossed-claisen condensation when one of the ketone or easter do not have any alpha hydrogens.

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Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 19.3, Problem 19.5P

Interpretation Introduction