OH is a very poor leaving group. However, many alcohols react with alkyl or aryl sulfo-nyl chlorides to give sulfonate esters.R-OH + R'-C -R,N>R-O-S-R' + HCI Suggest the product of the following reaction.CH,CH,-0-S-C,H; + CH,S¯N *DMSO

Concept introduction; SN2 reaction: The rate of substitution reaction depended on both substrate and…

Answered: OH is a very poor leaving group.…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

See similar textbooks

Similar questions

1.Write the product of 4-chloro-1-hexyne with the following reagents a) ---1.BH3 2.H2o2, - OH---> b) ---2 HBr--> c) ---H2O,H2SO4, HgSO4-->
These reagents can produce ketones with alkynes A. BH3, THF, H2O2 B. KMnO4 C. O3 D. H2SO4, H2O, HgSO4
Predict the products of reaction of pent-1-yne with the following reagents. warm, concd. KMnO4, NaOH
For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2) hydroboration–oxidation.(a) hex-1-yne
We are asked to prepare (CH3)2CHCH2OH (2- methylpropan-1-ol) from an alkyl halide and any required reagents ?
Oximene and myrcene, two hydrocarbons isolated from alfalfa that have the molecular formula C10H16, both yield 2,6- dimethyloctane when treated with H2 and a Pd catalyst. Ozonolysis of oximene forms (CH3)2C = O, CH2 = O, CH2(CHO)2, and CH3COCHO. Ozonolysis of myrcene yields (CH3)2C = O, CH2 = O, (two equiv), and HCOCH2CH2COCHO. Identify the structures of oximene and myrcene.
what is the product of 1-Hexyne reacting with 1 equivalent of HBr? Include E/Z if necessary.
Give the major product for the reaction. (CH3)2CHCHBrCH3 + -OC(CH3)3
Draw the substitution product formed (including stereochemistry) when (R)-hexan-2-ol is treated with each series of reagents: (a) NaH, followed by CH3I; (b) TsCl and pyridine, followed by NaOCH3; (c) PBr3, followed by NaOCH3. Which two routes produce identical products?
What are the reaction products of (R)-3-methylcyclohexene in the reaction sequence of hydroboration-oxidation: I- (1S,2R)-2-methylcyclohexanol + (1R,2R)-2-methylcyclohexanol, barely II- (1S,2R)-2-methylcyclohexanol + (1R,2S)-2-methylcyclohexanol, barely III- (1S,3R)-3-methylcyclohexanol + (1R,3R)-3-methylcyclohexanol, barely IV- (1S,3R)-3-methylcyclohexanol + (1S,3S)-3-methylcyclohexanol, barely V- Alternatives I and III contain the reaction products VI- nda
What is the major product of the reaction of 1 mol of propyne with each of the following reagents? a. HBr (1 mol) e. aqueous H2SO4, HgSO4 h. H2/Lindlar catalyst b. HBr (2 mol) f. R2BH in THF followed by i. sodium amide c. Br2 (1 mol)/CH2Cl2 H2O2/HO-/H2O j. the product of part i followed by d. Br2 (2 mol)/CH2Cl2 g. excess H2, Pd/C 1-chloropropane
Draw a structural formula for the product of each SN2 reaction. Where configuration of starting material is given, show the configuration of the product, (CH3)3N + CH3I in the presence of acetone = ?

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS

OH is a very poor leaving group. However, many alcohols react with alkyl or aryl sulfo- nyl chlorides to give sulfonate esters. R-OH + R'- C - R,N >R-O-S-R' + HCI Suggest the product of the following reaction. CH,CH,-0-S-C,H; + CH,S¯N * DMSO