4. Provide the required starting reactant that would be expected to produce the shown product(s) when treated with the indicated reagents. a. b. C. d. e. f. 1. LIAIH 2. H₂O H2 Lindlar's catalyst 1. 03 2. CH3SCH3 1. CH3MgBr 2. H₂O (CH3)3COOH Ti(OCH(CH3)2]4 (+)-diethyl tartrate 1. LiAlH4 2. H₂O H3CH2C H3CH2C HO OH OH ° CH3 CH₂OH CH2CH2CH3 H3CH2C H3CH2C H CH3

4. Provide the required starting reactant that would be expected to produce the shown product(s) when treated with the indicated reagents. a. b. C. d. e. f. 1. LIAIH 2. H₂O H2 Lindlar's catalyst 1. 03 2. CH3SCH3 1. CH3MgBr 2. H₂O (CH3)3COOH Ti(OCH(CH3)2]4 (+)-diethyl tartrate 1. LiAlH4 2. H₂O H3CH2C H3CH2C HO OH OH ° CH3 CH₂OH CH2CH2CH3 H3CH2C H3CH2C H CH3

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

Reagents a. HBr m. 2 equivalents of NaNH2 b. HBr, H2O2, hv c. H20, H2SO4 d. Br2 H2, Lindlar's catalyst Na / NH3 H2SO4, H9SO4 (sia)2BH then H2O2, NaOH n. O. 5 р. е. Cl q. 1 equivalent of NANH2 H2, Pd g. Br2, H2O h. Cl2, H2O OsO4 then NaHSO3 j. Hg(OAc)2, H2O then NABH4 k. BH3 then H2O2, NaOH Og then (CH3)2S f. r. S. NBS, hv Br2, hv Cl2, hv t. i. u. V. HCI I. 2 Previous Next
select reagents: cyclopentanone Reagents a. C6H5CHO b. NaOH, ethanol c. Pyrrolidine, cat. Hj. d. H₂C=CHCN e. H3O+ f. LDA g. A) bg EtOC(=O)CO₂Et h. i. B) ka k. I. m. O: BrCH₂CH=CH₂ NatOEt, ethanol Br₂, H+ K+ t-BUO™ CH2(CO2Et)z heat C) jh CO₂Et D) Im
Give the organic reaction products for the following reaction a. b. a. b. CH3CH2-C. ง ว NaOH ? + ? N(CH3)2 H₂O H*/H₂O CH3-C-OCH2CH3 ? + ?
1. Alcohols X and Y formed layers with Lucas reagent. Compound X formed brown precipitate with KMnO4 while compound Y did not. Which are the possible identities of compounds X and Y? a.tert-butanol, propanol b.isopropanol, isopentyl alcoholc. methanol, ethanold.tert-butanol, isopropanol2. Alcohols that cannot be distinguished using the Lucas test? a.isopropanol and methanol b.t-butyl alcohol and ethanol c.t-butyl alcohol and 2-methylbenzyl alcohol d.ethanol and n-propanol
3. What should be removed from the reactive media for the reaction below to obtain high conversion? n H3C-O-C- A. Ethylene glycol B. Methanol C. Ethanol D. Dimethyl ester of terephthalic acid CH3 + n HO–CH2CH2OH + 2л CH3OH
6.Give the major organic product(s) of the following reactions. nily CH, Н.С Н.С a. + H2O 1. (CH),CHCH,MgBr. Et0 2 Н.о b. н.с CH3 KMNO4 C. Но"
H2C=CHCH=CH2 H2NCH,CH2CH2CH2CH2CH,NH2 Reagents a. Br2, CH2CI2 КCN, HCN b. LIAIH, then H3o* H2, Pd/C excess NBS, CCI4 excess CH3MgBr, ether then H3O* H3O*, heat C. d. е. f. g. Select reagents from the table to carry out this transformation. (Enter your answer as a single string of letters representing the reagents in the order that you wish to use them, i.e. bdce.)
Which of the following compounds can be used to synthesize ethanoicpropanoic anhydride (CH;COOOCCH½CH3)? A. CH;COCI+ CH;CH2COO`Na* → B. CH;COOH +heat → C. CH3CH2CH2COCI + CH;COO Na* → D. A and C
Give the structure of the major organic product for the reaction sequence shown.
OCH3 CH3 c-H Determine the product formed when the given compound is reacted with the reagent given below Choose from the following: A. В. C. D. E. OCH3 OCH3 OCH; CH2OCH3 CH,OH HO HO HO HO CH; `CH3 CH3 `CH;OH CH;´ `CH2OH CH;´ `CH;OH CH3 `CH;OH Reagent: excess H2, metal catalyst
Br CH3 Br2 CH3CHCHCH2ČHCH3 Br OH 1. Hg(OAc)2, H20 2. NABH4 CH3CH2CH2CHCH3 HCI CH3CHCHCH2CH2CH2CH3 ČH3 CH3 -CH3 H/Pd
Reactions: Provide the structure(s) of the expected major organic product(s). Show stereochemistry where needed and write NR if there is no reaction. C. a. b. OH Br NaBr 1. TsCl, Pyridine 2. NaCN, DMSO CH3OH