
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Transcribed Image Text:个
Draw the organic product of the Lewis acid-base reaction
shown below. Include all lone pairs and charges as appropriate.
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F1
BF3
Select to Draw
F2
90
F3
900
000
F4
F5
Problem
F6

Transcribed Image Text:Draw a resonance structure that places a pi bond in a different
position. Include all lone pairs in your structure.
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F1
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2
F2
#3
3
20
F3
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4
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F5
A
6
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- Please helparrow_forward7. Now circle the lewis acid and lewis base sites on the following compounds. Some compounds may have both or just one. Note you can use LA for lewis acid and LB for lewis base as labels. S-H H.arrow_forwardDraw the organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. HCI Drawing C:Oarrow_forward
- Draw the organic product of the Lewis acid-base reaction shown below. Include all lone pairs and charges as appropriate. :O: BF3 Select to Draw Please select a drawing or reagent from the question areaarrow_forwardDraw the major organic oduct of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. HO NaOH :0: -0:0 Qarrow_forwardhelp please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all workingarrow_forward
- 6. Rank the indicated a-H's from most to least acidic (most acidic= 1). Be sure to explain your rankings for each by drawing significant resonance structures for the conjugate base and commenting on any other factors that contribute to your rankings. H H H H. A B Cmpd Rank Resonance Structures Reasoning A Вarrow_forwardDraw the mechanism showing the Brønsted acid/base reaction between propanoic acid and methylamine. Label the acid, base, conjugate base, and conjugate acid. Show all curved arrows, lone pairs and nonzero formal charges. einedoelM HO, CH;NH, propanoic acid pKa = 4.9 methylamine Mechanism: Using the pKa information provided/pKa tables (table appended to the end of this document), determine whether the starting reagents (propanoic acid and methyl amine) or resulting products would be favored at equilibrium (no math needed!).arrow_forward#2arrow_forward
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