QUESTION 11 Which one is a wrong statement about the intermediate of nucleophilic acyl subsitution? The intermediate is a result of forming a new T bond. The step in mechanism after intermediate formation is reforming carbonyl group and loss of leaving group. O it is a tetrahedral intermediate. In the intermediate, O from carbonyl group is negatively charged. After nucleophilic attack step, the attacked carbon in the intermediate has sp hybridization. O O O
QUESTION 11 Which one is a wrong statement about the intermediate of nucleophilic acyl subsitution? The intermediate is a result of forming a new T bond. The step in mechanism after intermediate formation is reforming carbonyl group and loss of leaving group. O it is a tetrahedral intermediate. In the intermediate, O from carbonyl group is negatively charged. After nucleophilic attack step, the attacked carbon in the intermediate has sp hybridization. O O O
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:QUESTION 11
Which one is a wrong statement about the intermediate of nucleophilic acyl subsitution?
The intermediate is a result of forming a new m bond.
The step in mechanism after intermediate formation is reforming carbonyl group and loss of leaving group.
O it is a tetrahedral intermediate.
In the intermediate, O from carbonyl group is negatively charged.
After nucleophilic attack step, the attacked carbon in the intermediate has spi hybridization.
Transcribed Image Text:QUESTION 12
When reacting 2.137 g of salicylic acid (CHgOa molar mass 138.12 g/mol) with 4.84 ml of acecic anhydride (C HOs molar mass
102.04 g/mol, density 1.082 g/mL). 2.117g of aspirin (CgH2O molar mass 180.15 g/mol) is formed. The percent yield of this
reaction is
Note: Input both numerical value and percentage mark. Pay attention to significantgures.
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