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4. Propose a mechanism for the formation of the following products OH +OH Br 5. Draw...
5. Propose a mechanism to justify the formation of the following product. (4) Br 1. NaNH2, Liq NH3
85. a. Propose a mechanism for the following reaction: in Br CHO Có + Br b. A small amount of a product containing a six-membered ring is also formed. Draw the structure of that product c. Why is so little six-membered ring product formed?
4)Draw stepwise mechanism that will explain the products of the following reaction. 5)draw the rate law and the transition state for the following reaction 6)what starting material would exclusively give you the product shown? Draw the mechanism using a chair structure. 4) Draw a stepwise mechanism that will explain the products of the following reaction on the back of this page. (6 points) 5) Draw the rate law and the transition state for the following reaction: (4 pts) DMSO CH;CH...
Draw a detailed mechanism for the following transformation 1. Br. Br HBr HO 2. What are the major product (s) formed in the following substitution reaction? Draw as Fisher projections CH;CH2ОH CH-CHз Нас— вr CH2CH2CH3 Draw the mechanism for the following reaction. 3. HO Br Draw the major organic product(s) produced in the following reaction as Fischer projection. 4. CHз ОСHЗ Н NaN3 Н. -CH3 Н- Br DMSO CH3 Draw the mechanism for the following reaction to demonstrate how the...
4. Predict the products of the following reactions & indicate whether they are most likely to go through an SN2, SN1, E1, or E2 mechanism. NaCN DMSO NaOH CH3OH heat Only one product is formed in the following E2 elimination reaction. Draw an arrow-pushing mechanism for the reaction and provide the correct product structure. Include a 3-D drawing (chair conformation) displaying proper stereochemistry of the transition state to explain formation of only the major product. CH3 •Br NaOCH3 ~"'CHS
Propose a mechanism for the formation of Tri-iodomethane. That is the precipitate formed in the positive reactions for methyl ketones. DO NOT USE another halogen 2) + CHX3 RCH3 baseCHX3 X2 base R O R- H, alkyl, aryl X - Cl, Br,I You will have to hand draw another step or two in this general reaction to make the mechanism make sense. (10pts)
PROBLEM 5. Reaction Mechanism 1. Propose products (major/minor) and provide a detaile reaction mechanism to account for the formation of the major product. Use curved arrow notation to indicate electron flow. Also, draw a structure of the transition state that accounts for the formation of the major product HЕr он 0° C major minor transition state corresponding to the major product of 20 points
4. [12 pts] Propose mechanisms for the formation of all 3 products shown in the reaction below: (draw curved arrows, intermediates, and resonance structures if necessary. NO NEED FOR TRANSITION STATES! CH CH CH CH Br Heat CH,CH,OH OCH.CH Mechanism.14 points) Mechanism 2 points) Mechanism.3 14 points) 5. [14 pts] Provide the major products of reacting the alkene shown in the middle of the scheme below with all the reagents independently. Draw the products' structures in the corresponding table below...
Problem 1 (10 pts) Draw the major product (monoalkylation) and propose a mechanism for its formation. OCH3 (CH3)3CCI AICI: Problem 2 (10pts) Draw the major product of the following reactions. Brz FeBr3 a) HNO3 H2SO4 b) OH ON NOZ NaOH 50°C c) Br Problem 3 (10 pts) Show the necessary steps for each of the following transformations. CO2H ŞO3H NO2 Br a) b)
Propose a mechanism for the follo heat Br Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. Electron flow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new bond should be created H-Br: Cl H-Br: H20