Most acidic protons needed to be found in the given anti-viral drug rilpivirine. Concept introduction: Acidic strength of the molecule depends on the stability of the Conjugate anion. If the conjugate anion is more resonance stabilized, the acid considered as strong acid, the anion is weak base and the removed proton considered as a strong acidic proton. If the negative charge present in the structure is more delocalized and stabilized by more number of atoms (electronegative), then the corresponding proton considered as more acidic proton. To give: the two most acidic protons in the antiviral drug, and give the most acidic between them.

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Answer 1

Question

Chapter 3, Problem 59IP

Interpretation Introduction

Interpretation:

Most acidic protons needed to be found in the given anti-viral drug rilpivirine.

Concept introduction:

Acidic strength of the molecule depends on the stability of the Conjugate anion.

If the conjugate anion is more resonance stabilized, the acid considered as strong acid, the anion is weak base and the removed proton considered as a strong acidic proton.

If the negative charge present in the structure is more delocalized and stabilized by more number of atoms (electronegative), then the corresponding proton considered as more acidic proton.

To give: the two most acidic protons in the antiviral drug, and give the most acidic between them.

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Answer 2

Question

Chapter 3, Problem 59IP

Interpretation Introduction

Interpretation:

Most acidic protons needed to be found in the given anti-viral drug rilpivirine.

Concept introduction:

Acidic strength of the molecule depends on the stability of the Conjugate anion.

If the conjugate anion is more resonance stabilized, the acid considered as strong acid, the anion is weak base and the removed proton considered as a strong acidic proton.

If the negative charge present in the structure is more delocalized and stabilized by more number of atoms (electronegative), then the corresponding proton considered as more acidic proton.

To give: the two most acidic protons in the antiviral drug, and give the most acidic between them.

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Answer 3

Question

Chapter 3, Problem 59IP

Interpretation Introduction

Interpretation:

Most acidic protons needed to be found in the given anti-viral drug rilpivirine.

Concept introduction:

Acidic strength of the molecule depends on the stability of the Conjugate anion.

If the conjugate anion is more resonance stabilized, the acid considered as strong acid, the anion is weak base and the removed proton considered as a strong acidic proton.

If the negative charge present in the structure is more delocalized and stabilized by more number of atoms (electronegative), then the corresponding proton considered as more acidic proton.

To give: the two most acidic protons in the antiviral drug, and give the most acidic between them.

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Answer 4

Question

Chapter 3, Problem 59IP

Interpretation Introduction

Interpretation:

Most acidic protons needed to be found in the given anti-viral drug rilpivirine.

Concept introduction:

Acidic strength of the molecule depends on the stability of the Conjugate anion.

If the conjugate anion is more resonance stabilized, the acid considered as strong acid, the anion is weak base and the removed proton considered as a strong acidic proton.

If the negative charge present in the structure is more delocalized and stabilized by more number of atoms (electronegative), then the corresponding proton considered as more acidic proton.

To give: the two most acidic protons in the antiviral drug, and give the most acidic between them.

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Answer 5

Chapter 3, Problem 59IP

Interpretation Introduction

Interpretation:

Most acidic protons needed to be found in the given anti-viral drug rilpivirine.

Concept introduction:

Acidic strength of the molecule depends on the stability of the Conjugate anion.

If the conjugate anion is more resonance stabilized, the acid considered as strong acid, the anion is weak base and the removed proton considered as a strong acidic proton.

If the negative charge present in the structure is more delocalized and stabilized by more number of atoms (electronegative), then the corresponding proton considered as more acidic proton.

To give: the two most acidic protons in the antiviral drug, and give the most acidic between them.

Answer 6

Chapter 3, Problem 59IP

Interpretation Introduction

Interpretation:

Most acidic protons needed to be found in the given anti-viral drug rilpivirine.

Concept introduction:

Acidic strength of the molecule depends on the stability of the Conjugate anion.

If the conjugate anion is more resonance stabilized, the acid considered as strong acid, the anion is weak base and the removed proton considered as a strong acidic proton.

If the negative charge present in the structure is more delocalized and stabilized by more number of atoms (electronegative), then the corresponding proton considered as more acidic proton.

To give: the two most acidic protons in the antiviral drug, and give the most acidic between them.

Answer 7

Chapter 3, Problem 59IP

Interpretation Introduction

Interpretation:

Most acidic protons needed to be found in the given anti-viral drug rilpivirine.

Concept introduction:

Acidic strength of the molecule depends on the stability of the Conjugate anion.

If the conjugate anion is more resonance stabilized, the acid considered as strong acid, the anion is weak base and the removed proton considered as a strong acidic proton.

If the negative charge present in the structure is more delocalized and stabilized by more number of atoms (electronegative), then the corresponding proton considered as more acidic proton.

To give: the two most acidic protons in the antiviral drug, and give the most acidic between them.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 3.2 - Prob. 1LTS Ch. 3.2 - All of the following acid-base reactions are...Ch. 3.2 - Prob. 2PTS Ch. 3.2 - Prob. 3ATS Ch. 3.3 - Prob. 2LTS Ch. 3.3 - Prob. 4PTS Ch. 3.3 - Prob. 5ATS Ch. 3.3 - Prob. 6ATS Ch. 3.3 - Prob. 3LTS Ch. 3.3 - Prob. 7PTS

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Chapter 3 Solutions