### Analysis of Reaction Mechanisms: SN1 vs SN2Each pair of reactions shown will proceed by the same mechanism, either SN1 or SN2. Your task is to identify the mechanism and determine which reaction in each pair proceeds faster, if any.#### Reaction Pairs:1. **First Pair:** - **Reaction 1:** \[ \text{CH}_3\text{Br} + \text{N}_3^- \to \text{CH}_3\text{N}_3 + \text{Br}^- \] - **Reaction 2:** \[ \text{CH}_3\text{OH} + \text{N}_3^- \to \text{CH}_3\text{N}_3 + \text{OH}^- \] - **Mechanism:** ________________ - **Faster 1 or 2 or Same? Why?**2. **Second Pair:** - **Reaction 1:** \[ \begin{aligned} &\begin{matrix} &\text{Cl} & &\text{+} &\text{OH}^- &\to & &\text{Cl} \\ &\vert & & & & &\vert \\ &\text{CH}_3 & & & & &\text{OH} \\ &\vert & & & & &\vert \\ &\text{CH}_2 & &+ & & &\text{CH}_2 &\\ &\vert & & &\text{OH}^- &\to &\vert \\ &\text{Cl} & & & & &\text{CN} \end{matrix} \end{aligned} \] - **Reaction 2:** \[ \begin{aligned} &\begin{matrix} &\text{Cl} & &\text{+} &\text{CN}^- &\to & &\text{Cl} \\ &\vert & & & & &\vert \\ &\text{CH}_3 & & & & &\text{CN} \\ &\vert & & & & &\vert \\ &\text{CH}_2 & &+ & & &\text{CH

According to the bartleby guidelines for the multipart questions, I can solve only first three…

1 2 1 2 1 1 2 1 2 H₂C 2 1. Each pair of reactions, 1 and 2, will both go by the same mechanism, Sn1 or Sn2, say which. Also, say which of the two in each pair do you expect to go faster, or the same, and why. 2 CH₂Br + CH₂OH + H₂C CH₂ -CI CH₂ CH₂ H₂C -CI CH3 CI + OH e CH₂ N₂ CN CI CH,S acetone CH,S CH,OH 8 Br CH₂NH H₂O H₂C- EtOH H₂O, CH₂OH CI H₂O, CH,OH NaOCH₂ acetone CH₂N₂ + CH3 CHs H₂C -SCH₂ Br CHÍNH DMSO NaOCH3 acetone CH3N3 + OH CH3 EtOH, H₂O -SCH3 CH3 OH CN + OH O Br OEt H₂C CH₂ OCH3 OH + + ci + HI + HI HCT OH + HC1 OCH3 + NaCl NHCH3 + Br O NHCH3 + Br + NaCl Mechanism Faster 1 or 2 or Same? Why? Mechanism Faster 1 or 2 or Same? Why? Mechanism Faster 1 or 2 or Same? Why? Mechanism_ Faster 1 or 2 or Same? Why? Mechanism_ Faster 1 or 2 or Same? Why? Mechanism Faster 1 or 2 or Same? Why? Mechanism Faster 1 or 2 or Same? Why?

1 2 1 2 1 1 2 1 2 H₂C 2 1. Each pair of reactions, 1 and 2, will both go by the same mechanism, Sn1 or Sn2, say which. Also, say which of the two in each pair do you expect to go faster, or the same, and why. 2 CH₂Br + CH₂OH + H₂C CH₂ -CI CH₂ CH₂ H₂C -CI CH3 CI + OH e CH₂ N₂ CN CI CH,S acetone CH,S CH,OH 8 Br CH₂NH H₂O H₂C- EtOH H₂O, CH₂OH CI H₂O, CH,OH NaOCH₂ acetone CH₂N₂ + CH3 CHs H₂C -SCH₂ Br CHÍNH DMSO NaOCH3 acetone CH3N3 + OH CH3 EtOH, H₂O -SCH3 CH3 OH CN + OH O Br OEt H₂C CH₂ OCH3 OH + + ci + HI + HI HCT OH + HC1 OCH3 + NaCl NHCH3 + Br O NHCH3 + Br + NaCl Mechanism Faster 1 or 2 or Same? Why? Mechanism Faster 1 or 2 or Same? Why? Mechanism Faster 1 or 2 or Same? Why? Mechanism_ Faster 1 or 2 or Same? Why? Mechanism_ Faster 1 or 2 or Same? Why? Mechanism Faster 1 or 2 or Same? Why? Mechanism Faster 1 or 2 or Same? Why?

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

Bromomethylcycloheptane has been prepared in 92% yield by the reaction that it shows. Write a stepwise mechanism and use curved arrows to indicate the flow of electrons. The reaction was carried out in water, so use H3O + as the donor of protons in its mechanism. Is the determining step of the speed unimolecular (SN1) or bimolecular (SN2)?
Which is a step in the mechanism of this reaction? (Note the product is purposefully not shown) HBr heat H H Br H H Br
Cycloaddition reactions are useful tools for building rings by using electrons to form o bonds between atoms. For the products below, identify a reasonable set of starting materials to make each product. NH₂ O g O Which of the two sets of starting materials you proposed above do you think would react more quickly? Think about what makes a cycloaddition fast or slow and justify your answer.
Consider the reaction of the molecule below with a nucleophile (Nu). Where will the nucleophile attack in the first step of the mechanism? 0000 A B D H3C A CO1CR с B D H₂ CH3
Use the two-step mechanism below to answer the following question. Step 1: NO (g) + N2O (g) → N2 (g) + NO2 (g) Step 2: 2 NO2 (g)→2 NO (g) + O2 (g) What is the intermediate? O N20 O NO O N2 NO2 O 02 MacBook Air DII 80 888 F6 F7 FB F3 F4 & %23 %24 3 4 5 8 E R Y F C в M I >
1. Which one of the following four schemes (A-D) represents a step in the mechanism of the reaction in the box? Cl2, light (hv) + HCI CỈ H Cl-H A B H C D H B OD OC O A
Draw the products and show the mechanism for the reactions below. Between each reactionpair indicate which one will proceed faster and explain why
Show the steps of this reaction
What is the mechanism of this reaction?
Which arrow best describes the mechanism for the reaction? B C D O A 台灣券 O B OD 2. SI O-0
Iodination of acetone reaction is shown by the following equation. CH3COCH3 + I2 ⟶ CH3COCH2I + HI Therefore, − d [ C H 3 C O C H 3 ] d t is a correct expression that can define the rate of the above reaction. Is this true or false?
Which mechanism will this reaction follow?