I deu But weekly, each one containing a few questions covering material from the previous week's lectures. The material on the sheets will be discussed at the tutorial sessions. Please revise your lecture notes on a weekly basis, do the necessary background reading and attempt the tutorial sheets. 1) a) Draw curved arrow(s) to show how aniline is converted to its resonance structure A and how resonance structure A is converted to resonance structure B. Draw the resonance structure C. Aniline A B b) The following resonance structures are used to describe the molecule diazomethane. It is a bright yellow, volatile, toxic, explosive and useful gas. H,C=N=N: H,C-N=N: Indicate the presence of any formal charges on these resonance structures by placing + and/or - signs above the appropriate atoms. Show all such charges in both structures. Insert curved arrows to show the interconversion between the above resonance structures. i.) ii.) iii.) Draw the resonance hybrid of the above resonance forms.

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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IDO BEGINNING ON MONDAY 8TH FEBRUARY, 2021.
DEASE COMPLETE YOUR TUTORIAL SHEET FOR DISCUSSIONS IN YOUR TUTORIAL
SESSIONS
NB: Tutorial sheets will be handed out weekly, each one containing a few questions covering material from
the previous week's lectures. The material on the sheets will be discussed at the tutorial sessions. Please revise
your lecture notes on a weekly basis, do the necessary background reading and attempt the tutorial sheets.
1) a) Draw curved arrow(s) to show how aniline is converted to its resonance structure A and how resonance
structure A is converted to resonance structure B. Draw the resonance structure C.
>
B
C
Aniline
b) The following resonance structures are used to describe the molecule diazomethane. It is a bright yellow,
volatile, toxic, explosive and useful gas.
H,C=N=N: +
H,C-N=N:
Indicate the presence of any formal charges on these resonance structures by placing + and/or
- signs above the appropriate atoms. Show all such charges in both structures.
Insert curved arrows to show the interconversion between the above resonance structures.
i.)
ii.)
iii.)
Draw the resonance hybrid of the above resonance forms.
Transcribed Image Text:IDO BEGINNING ON MONDAY 8TH FEBRUARY, 2021. DEASE COMPLETE YOUR TUTORIAL SHEET FOR DISCUSSIONS IN YOUR TUTORIAL SESSIONS NB: Tutorial sheets will be handed out weekly, each one containing a few questions covering material from the previous week's lectures. The material on the sheets will be discussed at the tutorial sessions. Please revise your lecture notes on a weekly basis, do the necessary background reading and attempt the tutorial sheets. 1) a) Draw curved arrow(s) to show how aniline is converted to its resonance structure A and how resonance structure A is converted to resonance structure B. Draw the resonance structure C. > B C Aniline b) The following resonance structures are used to describe the molecule diazomethane. It is a bright yellow, volatile, toxic, explosive and useful gas. H,C=N=N: + H,C-N=N: Indicate the presence of any formal charges on these resonance structures by placing + and/or - signs above the appropriate atoms. Show all such charges in both structures. Insert curved arrows to show the interconversion between the above resonance structures. i.) ii.) iii.) Draw the resonance hybrid of the above resonance forms.
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