The reaction shown in panel I of the figure is the formation a cyclic anhydride by attack of a carboxylate anion. Based on the rate information thereaction on top of I goes.than the reaction on the bottom of I and this is due toA-0 +ABRate at 1 M concentrations 4x 10* MsIncreasing rateof reaction(assume A and B reactupon sideways collsion)Rate 08 MisIIfaster, proximity effectB. more slowly, acid base catalysisfaster, orientation effectC.D.more slowly, proximity effectF. more slowly, orientation effect

The proximity effect is the ability of reaction to occur at a faster rate due to the presence of…

The reaction shown in panel I of the figure is the formation a cyclic anhydride by attack of a carboxylate anion. Based on the rate information the reaction on top of I goes_ _ than the reaction on the bottom of I and this is due to, • - A- . © Rate at 1 M concertrations *4x 10* Ms Increasing rate of reaction (assume A and 8 react upon sideways colision) Rate 08 Mis II O faster, proximity effect O B. more slowly, acid base catalysis oc faster, orientation effect O D. more slowly, proximity effect O E. more slowly, orientation effect

The reaction shown in panel I of the figure is the formation a cyclic anhydride by attack of a carboxylate anion. Based on the rate information the reaction on top of I goes_ _ than the reaction on the bottom of I and this is due to, • - A- . © Rate at 1 M concertrations 4x 10 Ms Increasing rate of reaction (assume A and 8 react upon sideways colision) Rate 08 Mis II O faster, proximity effect O B. more slowly, acid base catalysis oc faster, orientation effect O D. more slowly, proximity effect O E. more slowly, orientation effect

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

answeron bracket thanks
7. The following data were collected for the reaction: (CH;);CBr + OH- (CH),СОН + Вr- trial [(CH;) CBr] [OH] rate of reaction (mol L-' s-') 1 0.50 M 0.050 M 0.0056 1.00 M 0.050 M 0.011 3 1.00 M 0.10 M 0.011 4 1.50 M 0.050 M 0.017 Determine the form of the rate law and calculate k, the rate constant. You must include units with your answer! Feel free to use any space above to determine relative concentrations/rate, but it's not required.
g) A series of reduction experiments was carried out at a given temperature. The results are summarized in Table 2 below. Determine the rate law expression for this reaction. [ 12 Table 2-Experimental rate measurements [R] (mol L³) [Methan-1-ol] (mol L¹) Rate (mol L¹s¹) 0.100 0.100 2.40 x 10² 0.100 0.300 7.20x10² 0.300 0.100 2.16 x 10¹ h) Below are two proposed reaction mechanisms for this reaction. Explain which reaction mechanism is correct. [ (Let Box methan-1-ol; BA= methanal; B = methanoic acid, R = reducing agent) Mechanism 1 Mechanism 2 BH+R BA (slow) BH+R BA (fast) BA+RBOH (fast) BA+R BON (slow)
A3
Pls solve this question correctly instantly in 5 min i will give u 3 like for sure
For the gas phase isomerization of cis-cyanostyrene, cis-C6H5CH=CHCN_trans-C%HşCH=CHCN the rate constant at 677 K is 5.01x10-4 51 and the rate constant at 717 K is 3.39x10-35-1. What is the activation energy for this reaction? kJ/mol
Figure 8-2 1 H+ А. ET с. H30+ + M гхи prog ер он P. Ер ми гхи prog H₂O: В. Britt un ет гхи prog ГХИ соо prog - н H2:
The following initial rate data are for the reaction of tertiary butyl bromide with hydroxide ion at 55 °C: (CH3)3CB + OH → (CH3)3COH + Br Experiment [(CH3)3CB1],, M [OH], M Initial Rate, Ms-1 1 0.890 1.50x10-3 1.50x10-3 3.01x10-3 3.01x10-3 0.118 0.118 2 1.78 0.890 1.78 3 0.237 4 0.237 Complete the rate law for this reaction in the box below. Use the form k[A]j™[B]" , where '1' is understood for m or n and concentrations taken to the zero power do not appear. Don't enter 1 for m or n Rate = From these data, the rate constant is
Give the complete mechanism for the following reaction: CH3CH3 + Cl2 ----> CH3CH2CI + HCI Edit View Insert Format Tools Table 12pt v Paragraph v BIUAv ev T? v O words
4. Explain why the rate of formation of 1-azidopropane is different depending on which halopropane (X = F, Cl, Br, I) is used. Explain which halopropane will react fastest? ~X X = F, Cl, Br, I NaN №3 1-azidopropane
Draw the reaction mechanism and reactants needed to produce these products - for letter a, use mannich reaction to draw the mechanism
What is the correct mechanism ?