0. Compound A reacts with B in the presence of sodium hydride to give C as a major product. HO A Free Energy NH₂ Ph B ŌSO₂CF3 NaH, THF a) Provide a detailed mechanism for the formation of C and draw it in the box above. ( C b) Draw the reaction coordinate diagram of that reaction. Indicate with an arrow the rate- determining step of the reaction then draw its transition state: Reaction Coordinate The reaction rate observed was 5 x 10-2 M.s¹ when the concentrations of A and B were 0.2 M and 0.1 M respectively. Determine the rate of this reaction when the concentration of A and B are now 0.3 M and 0.2 M respectively. Show your work.

0. Compound A reacts with B in the presence of sodium hydride to give C as a major product. HO A Free Energy NH₂ Ph B ŌSO₂CF3 NaH, THF a) Provide a detailed mechanism for the formation of C and draw it in the box above. ( C b) Draw the reaction coordinate diagram of that reaction. Indicate with an arrow the rate- determining step of the reaction then draw its transition state: Reaction Coordinate The reaction rate observed was 5 x 10-2 M.s¹ when the concentrations of A and B were 0.2 M and 0.1 M respectively. Determine the rate of this reaction when the concentration of A and B are now 0.3 M and 0.2 M respectively. Show your work.

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

The mechanism that allows the exothermic hydrolysis of t-butyl chloride to form t-butyl alcohol and chloride ion is as follows: (CH3)3CCl → (CH3)3C+ + Cl− (CH3)3C+ + H2O → (CH3)3COH + H+ Draw the transition state for each step.
When benzyl bromide is treated separately with KI and CH3OH, the substitution products are different but the reaction rates are about the same. KI Br (a) What does this suggest about the mechanism-is it SN1 or SN2? Explain. (b) Draw the complete mechanism (including curved arrows) for the formation of each product. (c) If the concentration of KI were doubled, what would happen to the rate of the substitution reaction? HOCH3 ?
I need help please
1) Clearly draw the mechanism of the reaction of: a) Water with 0=SeCl2 to form O=Se(OH)2 b) Water with 0=SeCl2 to form SeO2 c) Methanol with POC13 to form PO(OMe)3 d) Methanol with P4O6 to form P(OMe)3 e) [S207]?- with HN(CH:)2 to form [SO3N(CH3)2]*
See image below
Draw the mechanism for the reactions below (include lone pairs on all structures; do not explicitly draw Hatoms in any products except aldehydes): H,N (b) H.
In the following reaction indicate its mechanism: 1° P(C6H5)3 (bromomethyl)cyclohexane 2° (CH3-CH2-CH, )Li
None
HO 11 N write down the mechanism and explain it.
Indicate the mechanism by which the following reaction occurs. Question 6 options: SN1 SN2 E1 E2 E1CB CI HCO₂H H₂O
I need help with the mechanism steps
I would like to understand how to mechanism of this reactions occur