Question A8There are two fundamental flaws (at least!) with the followed proposed transformation. Whatare they? Suggest a reasonable route for this conversion (C to D). (Hint: More than one stepwill be required.)NHNH2AICIJuestion A8HNQuestion A10Give the product from each of the following reaction and provide a chemically-rbasonablemechanism for the transformation. Ensure the stereochemistry of the product is clearlydisplayed.Heat

Reaction is already solved. In the question A8, first step is the protection of amine group as AlCL3…

Question AS There are two fundamental flaws (at leastl) with the followed proposed transformation. What are they? Suggest a reasonable route for this conversion (C to D). (Hint: More than one step will be required.) NH NH, Juestion A8 EtOH Question A10 Give the product from each of the following reaction and provide a chemicalty-reasonable mechanism for the transformation. Ensure the stereochemistry of the product is clearly displayed. Heat

Question AS There are two fundamental flaws (at leastl) with the followed proposed transformation. What are they? Suggest a reasonable route for this conversion (C to D). (Hint: More than one step will be required.) NH NH, Juestion A8 EtOH Question A10 Give the product from each of the following reaction and provide a chemicalty-reasonable mechanism for the transformation. Ensure the stereochemistry of the product is clearly displayed. Heat

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...

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Propose the reagents in best order for the synthesis of the following compound from benzene. CI A) B) 1) CH3CH2Cl, AlCl3 2) Cl₂, AlCl3 3) CH3COCI, AlCl3 1) CH3CH2Cl, AlCl3 2) CH3COCI, AlCl3 3) Cl₂, AlCl3 D) 1) CH3CH2Cl, AlCl3 2) Fuming H₂SO4 2) Cl₂, AlCl3 3) CH3COCI, AlCl3 4) Dilute H2SO4 E) C) 1) CH3COCI, AlCl3 2) Zn(Hg), HCl, Heat 3) Fuming H2SO4 4) Cl₂, AlCl3 5) Dilute H2SO4 1) CH3COCI, AlCl3 2) Cl₂, AlCl3 3) CH3CH2Cl, AlCl3 4) Zn(Hg), HCl, Heat
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7) Predict the major products of the following reactions, including stereochemistry where appropriate. DRAW the detailed structure of those products. a) sec-butyl isopropyl ether + concd. HBr / A b) ethyl phenyl ether + concd. HI / A c) trans-2,3-epoxyoctane + H₂O / H₂SO4 d) methyl phenyl ether + 1) BBr3 / THF 2) H₂O h) 1,2-epoxyhexane + CH₂OH / H₂SO4 i) epoxypropane + excess CH3NH2 j) potassium tert-butoxide + 1-bromobutane k) cis-2,3-epoxyoctane + HCl / Et₂O
Which of the following is a major product of the reaction shown? (CH3),CHCH;NH2 **** HN- H* (cat./H;0 (A) (B) N- (C) (D) Compound D OCompound C O Compound A Compound B
A common alkene starting material is shown below. Predict the major product for each reaction. Ignore any inorganic byproducts. Select to Select to Draw Draw mCPBA 1.03 2. H2O2 1.03 2. (CH3)2S nd 1.03 2. Zn/H3O+ I I
help; please DRAW IT; don't answer in text. thanks the reactions are all covered in Organic Chemistry, 6th Edition by Marc Loudon and Jim Parise. Chapter 15-17
14. Which reactant can be treated with 1) LiAlH4, 2) H2O to create the molecule shown below: H3C C -N- C CH3 Н2 H H₂ A) N-ethylethanamide (common name: N-ethylacetamide) B) ethanenitrile (common name: acetonitrile) C) ethanamide (common name: acetamide) D) butanenitrile
What epoxide and organometallic reagent are needed to synthesize each alcohol below? Pay close attention to the correct representation of stereochemistry, where appropriate. 3. (а) "OH desired ерохide organometallic reagent product (b) H но desired product ероxide organometallic reagent 4. A CHEM 245 student wants to synthesize some ethylene glycol to use as antifreeze in his radiator this winter. He proposes the following reaction to his instructor, who quickly explains that this reaction won't work as proposed due to the student's choice of reagent. 1) NaH 2) H2O OH Но a) Why can't sodium hydride (NaH) be used as the nucleophile in the reaction above? b) Propose an alternate reagent that COULD be used with the ethylene oxide to successfully give the desired ethylene glycol product.
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