NH₂CHEM 372 – Problem Set 15 - Organic redox & coenzymes8. Complete these resonance forms of NAD+, showing that the ring is electron poor and able toaccept a hydride (HT). There are many ways to draw the resonance relationships, but only certaincarbon sites will be shown to be cationic. You'll need to include the pi bonds and formal charges.+NH₂ONIRNIRNH₂NIRNIRNH ₂

Given question is based on resonance. Resonance structures are set of two or more Lewis structures…

CHEM 372 - Problem Set 15 - Organic redox & coenzymes 3. Complete these resonance forms of NAD+, showing that the ring is electron poor and able to accept a hydride (H). There are many ways to draw the resonance relationships, but only certain carbon sites will be shown to be cationic. You'll need to include the pi bonds and formal charges.

CHEM 372 - Problem Set 15 - Organic redox & coenzymes 3. Complete these resonance forms of NAD+, showing that the ring is electron poor and able to accept a hydride (H). There are many ways to draw the resonance relationships, but only certain carbon sites will be shown to be cationic. You'll need to include the pi bonds and formal charges.

Chemistry

10th Edition

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...

See similar textbooks

Similar questions

Draw a resonance form for 1 H-pyrrolo[2,3-b]pyridine in which nitrogen has a formal charge of +1. Be sure to include all lone pairs and charges in your structure. H : ☐ 5 00 ER o0o Ar HB Π
Using curved arrows, show the mechanism for the acid-base reaction. Be sure to show all lone pair electrons as well as non-zero formal charges. ·O· X X H X Ś +
4. What is the order of (i) boiling point; and, (ii) acidity for the following set of hydrogen compounds H₂O; H₂S; H₂Se; H₂Te a.H-SH < H-SeH < H-TeH < H-OH; H-OH <H -SH < H-SeH < H-TeH b. H-OH <H -SH < H-SeH < H-TeH; H-SH < H-SeH < H-TeH < H-OH c. H-SH < H-SeH < H-TeH < H-OH; H-SH < H-SeH < H-TeH < H-OH d. H-OH <H -SH < H-SeH < H-TeH; H-OH <H -SH < H-SeH < H-TeH 5. What are the bond angles of the lone pairs of in (i) acetone; and, (ii) water? a. 109.5°; 109.5° b. 109.5°; 120° c. 120°; 109.5° d. 120°; 120°
what are reagents x and y Hint: for x either Br, br2, or HBr; for y is an anion/alkoxide
LYRICA (pregabalin) is an oral pharmaceutical primarily indicated for the management of fibromyalgia and neuropathic pain. At a pH of 11, LYRICA has an overall charge of –1, with most atoms neutral and only one oxygen showing a –1 formal charge. The structure for LYRICA at pH 11 is shown below. Add all the missing lone pairs to the given structure of LYRICA.
Q 3 please
Propose a reasonable mechanism for the reaction, drawing out Lewis structure, using arrows to show electron flow, clearly identifying the bond making/bond breaking steps, and proposing reasonable intermediates for the reaction.
This is a Brønsted-Lowry acid-base reaction. Draw structures for all the products, showing any non-zero formal charges in each one. Make sure your reaction is balanced. Note for advanced students: Draw only the most stable resonance structure for each product. do NH, CH,-CH-CH-CH, HCI Click and drag to start drawing a structure. CH3
Draw a structural formula for the organic anion (i.e., do not include K+ or Nat) formed from the following reaction. Don't forget the charge on the ion. 0 сненансон CH3 CH4 +KOH →→ ? • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Include all nonzero formal charges. References to access important values if needed for this question. ? ChemDoodle Ⓡ Previous
Which of the following structures, including formal charges, is correct for diazomethane? H₂CNN: H₂C=N=N: H₂C N3 EN: H₂C=N= EN: +3 -3 7:2: H₂C-N- N:
None
Q 2 please