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D Question 6 1 pts Which of the structures is NOT a valid resonance contributor for the corresponding enolate of the following 1

D Question 6 1 pts Which of the structures is NOT a valid resonance contributor for the corresponding enolate of the following 1,3-diketone? U Ph a) b) Ph Ph d) o OH e) none of a), b), c) or d) e Ph a Ob Oc Od Oe + Previous Next →

D Question 6 1 pts Which of the structures is NOT a valid resonance contributor for the corresponding enolate of the following 1,3-diketone? U Ph a) b) Ph Ph d) o OH e) none of a), b), c) or d) e Ph a Ob Oc Od Oe + Previous Next →

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© Problem - 6.37 from textbook and Powerpoint missing Lone pairs and draw curved arrows for each step of the following mechanism Add for a pus with your Solution ond Explanation :0 POH Hic :0: :03 - CH3SO₃ A -In I Step St attack on carbon the double bond o

Organic Chemistry

Reactions of benzene Solutions

© Problem - 6.37 from textbook and Powerpoint missing Lone pairs and draw curved arrows for each step of the following mechanism Add for a pus with your Solution ond Explanation :0 POH Hic :0: :03 - CH3SO₃ A -In I Step St attack on carbon the double bond of benzene ring Shifts found as shown in the figure Final R=0 electrons of double bond Shiled to open In I Slep Negative charge having electrons on Oxygen Shifted to N-o bond then shifting of double bond occurs and finally electron of Co to oxygon as shown in Figure Band -CH320,8 becomes the leaving group and is removed = In I Stop 0-H bond breaks and Ht combine with Oh to release Hzo and compand D is formed as shown in figure + Z N bond goes 80: GOH -H₂O + 11 3

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Organic Chemistry

Reactions of benzene Solutions

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6. Predict the structure of the product for the following reaction and Draw the reaction mechanism for the reaction. Make sure to include electron arrows, electrophile formation, lone pair electrons and non-zero formal charges CI AICI:

Organic Chemistry

Reactions of benzene Solutions

6. Predict the structure of the product for the following reaction and Draw the reaction mechanism for the reaction. Make sure to include electron arrows, electrophile formation, lone pair electrons and non-zero formal charges CI AICI: