Resonance structure has to be drawn for the given compound. Concept introduction: Resonance structures: Resonance structures are electrically equivalent Lewis structures. Formal charges on these structures are same, these structures represented through a double headed arrow between the structures. Resonance structures are resulted during the delocalization of pi-electrons in the compound. To find: the resonance structure of the given compound.

Question

#1. Retro-Electrochemical Reaction: A ring has been made, but the light is causing the molecule to un- cyclize. Undo the ring into all possible molecules. (2pts, no partial credit) hv

Answer 1

Question

Chapter 2, Problem 59PP

(a)

Interpretation Introduction

Interpretation:

Resonance structure has to be drawn for the given compound.

Concept introduction:

Resonance structures: Resonance structures are electrically equivalent Lewis structures. Formal charges on these structures are same, these structures represented through a double headed arrow between the structures. Resonance structures are resulted during the delocalization of pi-electrons in the compound.

To find: the resonance structure of the given compound.

(b)

Interpretation Introduction

Interpretation:

Resonance structure has to be drawn for the given compound.

Concept introduction:

Resonance structures: Resonance structures are electrically equivalent Lewis structures. Formal charges on these structures are same, these structures represented through a double headed arrow between the structures. Resonance structures are resulted during the delocalization of pi-electrons in the compound.

To find: the resonance structure of the given compound.

(c)

Interpretation Introduction

Interpretation:

Resonance structure has to be drawn for the given compound.

Concept introduction:

Resonance structures: Resonance structures are electrically equivalent Lewis structures. Formal charges on these structures are same, these structures represented through a double headed arrow between the structures. Resonance structures are resulted during the delocalization of pi-electrons in the compound.

To find: the resonance structure of the given compound.

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#1. Retro-Electrochemical Reaction: A ring has been made, but the light is causing the molecule to un- cyclize. Undo the ring into all possible molecules. (2pts, no partial credit) hv

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I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."