QUESTION 1 A 1,2-methyl shift occurs when which of the following iodides is heated in ethanol? C6H5CHICH(CH3)2 (CН32CHCHICH3 (CH3)3CCHICH2CH3 (CH3)3CCH2CH21 (CH3)2C=CHI QUESTION 2 Which of the following reactions give the products shown under E2 conditions. Mark all correct a CH3CH major min or major min Br CH;0 major major minor minor Br 00000

QUESTION 1 A 1,2-methyl shift occurs when which of the following iodides is heated in ethanol? C6H5CHICH(CH3)2 (CН32CHCHICH3 (CH3)3CCHICH2CH3 (CH3)3CCH2CH21 (CH3)2C=CHI QUESTION 2 Which of the following reactions give the products shown under E2 conditions. Mark all correct a CH3CH major min or major min Br CH;0 major major minor minor Br 00000

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter89: Thin-layer Chromatography

Section: Chapter Questions

Problem 8P

See similar textbooks

Similar questions

Write equations for the reaction of 1-butanol with reagent. Where you predict no reaction, write NR. Q) K2Cr2O7, H2SO4, H2O, heat
(A true story.) A drug user responded to an ad placed by a DEA informant in a drug-culture magazine. He later flew fromColorado to Maryland, where he bought some 1-phenyl-2-propanone (P2P) from the informant. The police waited nearlya month for the suspect to synthesize something, then obtained a search warrant, and searched the residence. They foundthe unopened bottle of P2P; apparently, the suspect was not a good chemist and was unable to follow the instructions theinformant gave him. They also found pipes and bongs with residues of marijuana and cocaine, plus a bottle of methylamine hydrochloride, some muriatic acid (dilute HCl), zinc strips, flasks, and other equipment.(a) Assume you are consulting for the police. Show what synthesis the suspect was prepared to carry out, to provideprobable cause for the charge of attempting to manufacture a controlled substance.(b) Assume you are a member of the jury. Would you convict the defendant of attempting to manufacture a…
Answer the following questions based on the reaction scheme below. i) State reagent Q ii) Draw the structural formula for compound R, T, U and W
Give the reagents and reaction conditions necessary for the following conversions with the name of each compound. CH3CH2CONH2 ➡ CH3CH2NH2 CH3CH2NH2 ➡ CH3CH2OH
The following two questions are related: What addition products are possible when 1-methylcyclohexene is reacted with dilute acid (H+/H2O)? Select one or more: a. 2-methylcyclohexanol b. 1,6-hexadione c. Cycloheptanol d. 1-methylcyclohexanol e. Cyclohexylmethanol Which of the products above corresponds to the major product of the reaction? Select one: a. Cycloheptanol b. Cyclohexylmethanol c. 2-methylcyclohexanol d. 1-methylcyclohexanol
Question 4: The reaction of propylbenzene with NBS gives: 1-bromo-3-phenylpropane 2-bromo-1-phenylpropane 1-bromo-1-phenylpropane A mixture of all three of the above compound The reaction of 1-phenyl-1-propene with HBr gives: Question 2 options: 1-bromo-3-phenylpropane 2-bromo-1-phenylpropane 1-bromo-1-phenylpropane A mixture of all three of the above compounds Question 17: The pKa of cyclopentadiene is much smaller than typical for an allylic hydrocarbon. The best explanation for this observation is: Question 17 options: Cyclopentadiene is much more stable than expected. Cyclopentadiene is much less stable than expected. The cyclopentadienyl anion is aromatic. The cyclopentadienyl anion is antiaromatic.
Write an equation for the reaction of CH2=CHCH2CH3 with each of the following reagents: a. H2O, H+ b. KMnO4, OH- c. Oxygen (Combustion) Can you write it out please and thank you
Chlorination of 2-butanone yields two isomeric products, each having the molecular formula C4H7ClO. (a) What are these two compounds? (b) Write structural formulas for the enol intermediates that lead to each of these compounds. (c) Using curved arrows, show the flow of electrons in the reaction of each of the enols with Cl2.
Two isomeric materials are available for your use. They are: A. 2-methyl-2-pentene (CH3)2C=CHCH2CH3B. 2-ethyl-1-butene (CH3CH2)2C=CH2 Give the name/s only (structures not required) of the product for the reaction of (i) A and (ii) B with the reagents listed below. Your answers should be given using A1 -A10 and B1-B10 as indicators.Eg. the product for your first reaction should be stated as A1 = name of product etc. HBr HOBr Ozone (O3)/Zn B2H6/H2O2 N-bromosuccinimide KMnO4/ OH- Hg (OAc)2 CH3CO2OH (Peroxyacetic acid) H2/ Pd H2/Li/NH3
Two isomeric materials are available for your use. They are: A. 2-methyl-2-pentene (CH3)2C=CHCH2CH3B. 2-ethyl-1-butene (CH3CH2)2C=CH2 Give the name/s only (structures not required) of the product for the reaction of (i) A and (ii) B with the reagents listed below. Your answers should be given using A1 -A10 and B1-B10 as indicators.Eg. the product for your first reaction should be stated as A1 = name of product etc. 8. Peroxyacetic acid 9. Br2, 600 degrees Celsius H2/ Li/ NH3
#B: Methyl acetate has methoxy, -OCH3 as the remaining of the alcohol part in the ester. Isopropyl acetate has isopropoxy, -OCH(CH3)2 as the remaining of the alcohol part in the ester. -OCH(CH3)2 is more electron donating than the methoxy, -OCH3 group due to the presence of two electron-donating -CH3 group in the former. Hence saponification reaction of Isopropyl acetate is much slower than methyl acetate. Hence the rate of saponification of methyl acetate, CH3CCO2CH3 is 50 times greater than that for isopropyl acetate.
I know the answers are ester, carboxylic acid and ortho disbstitited phenyl, but i am missing one more. pls help Which of the following functional groups are present in 2-acetoxybenzoic acid? Group of answer choices aldehyde ester alcohol hydroxyl para-disubstituted phenyl nitro alkyl ketone carboxylic acid alkene meta-disubstituted phenyl ether amide ortho-disubstituted phenyl