Image upload answer is not allowed please dear expert Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of theexpected main organic product.1. TsCl,pyridineCH2CH2OH2. Br

Step 1:The condensed formula of the main organic product would be CH3CH2Br.Mechanism:- 1. Formation…

Answered: Consider the reaction between an…

Chemistry & Chemical Reactivity

10th Edition

ISBN:9781337399074

Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel

Publisher:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel

Chapter23: Carbon: Not Just Another Element

Section: Chapter Questions

Problem 109IL

See similar textbooks

Question

Image upload answer is not allowed please dear expert

Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of the
expected main organic product.
1. TsCl,pyridine
CH2CH2OH
2. Br

Expert Solution

Step by step

Solved in 2 steps with 1 images

SEE SOLUTION Check out a sample Q&A here

Similar questions

Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of the expected main organic product. CH₂CH₂CH₂OH 1. TsClpyridine 2. CT CH, CI Incorrect
Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of the expected main organic product. 1. TsCl.pyridine CH₂CH₂OH 2. NC
Identify the organic functional groups and reaction type for the following reaction.Please include everything including the letter and the answers.The reactant is a(n)a. amideb. aldehydec. alcohold. carboxylic acide. esterf. ketoneThe product is a(n)a. carboxlyate ionb. ammonium ionc. alcohold. carboxylic acide. ketonef. aldehydeThe reaction type isa. hydrationb. esterificationc. hydrolysis (in acid)d. hydrolysis (in base)e. amide synthesisf. amide synthesisg. dehydrationh. acid base
2. Some students confuse the ester and ether functional groups. Both linkages are formed by condensation reactions. a) Complete this statement: An ether linkage is formed by the condensation of: b) Use structures to show the condensation of cyclohexanol molecules to create the alternate synthesis product discussed in the report sheet of your Dehydration experiment (Lab 04).
Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of the expected main organic product. 1. TsCl.pyridine CH;CH,OH 2. CI
Identify the organic functional groups and reaction type for the following reaction if only the major product is shown.The reactant is a(n)a. alkyneb. etherc. alkened. alcohole. aromaticThe product is a(n)a. tertiary alcoholb. primary alcoholc. aldehyde d. ethere. secondary alcoholThe reaction type is :a. hydrolysisb. hydrationc. reduction (hydrogenation)d. dehydratione. oxidationI got alkene, tertiary alcohol, and hydrolysis, but I missed one of them. What are the correct answers?
Identify the organic functional groups and reaction type for the following reaction if only the major product is shown.The reactant is a(n)a. alkyneb. etherc. alkened. alcohole. aromaticThe product is a(n)a. tertiary alcoholb. primary alcoholc. aldehyded. ethere. secondary alcoholThe reaction type is :a. hydrolysisb. hydrationc. reduction (hydrogenation)d. dehydratione. oxidation
6. Write the structure of the following compounds. a. 4 - ethyl - 2 - hexoneb. 2-ethyl - 3 – pentanoic acid
4. Draw the line structure for the ester that can be formed from the reaction of the acid anhydride and the alcohol given below. :0: :0: HO CH3-CH2-C-o-C-CCH2-CH3 acid anhydride alcohol
Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of the expected main organic product. CH3OH −→−−−−−−−−2. CH3S−1. TsCl,pyridine
II. Give the condensed structural formula of each of the following ethers. 1. Isopropyl propyl ether 2. Methyl phenyl ether 3. 3-Methoxyhехane 4. 3-Methyl-2-isopropoxypentane 5. Ethoxycyclobutane
. The following chemical reactants produce the ester ethylethanoate (C4H8O2):C2H6O + CH3COOHWhat type of reaction occurs to make ethyl ethanoate?a. condensationb. hydrolysisc. combustiond. acid-base reaction

SEE MORE QUESTIONS

Recommended textbooks for you

Chemistry & Chemical Reactivity

Chemistry

ISBN:

9781337399074

Author:

John C. Kotz, Paul M. Treichel, John Townsend, David Treichel

Publisher:

Cengage Learning

Chemistry & Chemical Reactivity

Chemistry

ISBN:

9781133949640

Author:

John C. Kotz, Paul M. Treichel, John Townsend, David Treichel

Publisher:

Cengage Learning

Chemistry & Chemical Reactivity

Chemistry

ISBN:

9781337399074

Author:

John C. Kotz, Paul M. Treichel, John Townsend, David Treichel

Publisher:

Cengage Learning

Chemistry & Chemical Reactivity

Chemistry

ISBN:

9781133949640

Author:

John C. Kotz, Paul M. Treichel, John Townsend, David Treichel

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS

Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of the expected main organic product. 1. TsCl,pyridine CH2CH2OH 2. Br