Show how you would use the Williamson ether synthesis to prepare the following ether. you may use any alcohols as your organic starting materials (a) cyclohexyl propyl ether (b) isopropyl methyl ether (d) ethyl n-propyl ether (two ways) (C) 3-butoxy-1,1-dimethylcyclohexane from 3,3-dimethyl-cyclohexanol and butanol.

Show how you would use the Williamson ether synthesis to prepare the following ether. you may use any alcohols as your organic starting materials (a) cyclohexyl propyl ether (b) isopropyl methyl ether (d) ethyl n-propyl ether (two ways) (C) 3-butoxy-1,1-dimethylcyclohexane from 3,3-dimethyl-cyclohexanol and butanol.

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter54: Photoreduction Of Benzophenone And Rearrangement Of Benzopinacol To Benzopinacolone

Section: Chapter Questions

Problem 3Q

See similar textbooks

Similar questions

9. Plan syntheses of the following compounds. You may use the given starting material and any compound containing three or fewer carbons. (a) (b) (c) (d) by Br or Br H Br H OH = OH
Which of the following synthesis reactions of organohalide occurs via electrophilic addition? (A) reaction of chlorine with propane B reaction of chlorine with propene reaction of thionyl chloride with propan-2-ol (D) all choices
Provide the structure of the major product(s) of the followings organic reactions: a) b) c) d) e) f) h) -CEC -CECH -CECH -CECH Na CH3CH₂-CEC-CH3 -CECH NaNH, H₂ Lindlar's catalyst Na NH3 HBr (1 equivalent) HgSO4 H₂SO4, H₂O Sia₂BH H₂O₂ он 1) 0₂ 2) H₂O Br H30
Question: Which reaction would be the best synthesis of the following compound? CH3-CH- NH- CH2- CH3 CH3 (a) (b) EtOH CH3-CH-Br + CH3-CH2- NH2 EtOH CH3-CH=CH2 + CH3-CH2- NH2 CH3 (c) (d) EtOH EtOH CH3-CH-Br + CH3-CEN CH3- CH-NH, + CH3-CHy- Br CH3 CH3 (A) (В) (D) Question: What is the IUPAC name for (СН3)3ССН(ОН)CH2CH(OH)CH2CH(C НЗ)2? * 1,1,1,6-tetramethyl-2,4-heptanediol 2,2,7-trimethyl-3,5-octanediol 2,2,6,6-tetramethyl-3,5-heptanediol 2,7,7-trimethyl-4,6-octanediol O O
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
Give the major organic product of the following reaction. 1) ВН3/THF 2) NaOH, H2O2 HO OH HO- OH There is no reaction under these conditions or the correct product is not listed here.
how how you would synthesize the following compounds, starting with benzene or toluene and any necessary acyclicreagents. Assume para is the major product (and separable from ortho) in ortho, para mixtures. 1-phenylpropan-2-ol
Provide the necessary reactants to make these following transformations/l 1) 2) 3) H3C-5 H OH NH₂ H₂C OH NH₂ OH
Draw structural formulas for the isomeric carbocation intermediates formed on treat- ment of each alkene with HCl. Label each carbocation 1°, 2°, or 3° and state which of the isomeric carbocations forms more readily. CH₂CH3 (a) H₂C=C (c) CH3 CH3 (b) (d) H₂C-CH=CH-CH3
What reagents would you use to carry out the following reaction? (A) H₂ / Pt (B) (C) (D) H₂/Lindlar's ??? Li, EtNH₂ followed by NH4Cl H₂O₂ / NaOH
Devise a synthesis of the ketone hexan-3-one, CH3CH2COCH2CH2CH3, from CH3CH2Br as the only organic starting material; that is, all the carbon atoms in hexan-3-one must come from CH3CH2Br. You may use any other neededreagents.
Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict themajor products of the reactions of naphthalene with the following reagents.(a) HNO3, H2SO4 (b) Br2, FeBr3 (c) CH3CH2COCl, AlCl3