EBK EXPERIMENTAL ORGANIC CHEMISTRY: A M
6th Edition
ISBN: 9781305687875
Author: Gilbert
Publisher: CENGAGE LEARNING - CONSIGNMENT
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Question
Chapter 9.3, Problem 2E
Interpretation Introduction
Interpretation: The requirement of light for bromination to occur with some of the hydrocarbons is to be described.
Concept introduction: Free radicals are uncharged molecules having an unpaired valence electron. These are typically highly reactive and short-lived molecules.
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20.
Outline the synthesis of
(a)
2-butanol from butane
(b)
2-bromo-3-methylbutane from 3-methyl-2-butanol
(b) Ozonolysis process was carried out towards an unknown organic
compound, X, to produce propanal, C3H6O and compound Y. Propanal was
then further oxidized into compound z, C3H6O2 by using potassium
permanganate, KMNO4 under acidic condition and heating. As an
alternative, compound Y can be produced from the reaction of benzene
with ethanoyl chloride, CH3COCI with the presence of aluminium trichloride,
AICI3.
Proses ozonolisis telah dijalankan terhadap sebatian organik yang tidak
dikenali, X untuk menghasilkan propanal, C3H6O dan sebatian Y. Propanal
kemudiannya dioksidakan menjadi sebatian Z menggunakan KMNO4 dalam
keadaan berasid dan panas. Sebagai alternatif, sebatian Y boleh dihasilkan
daripada tindak balas antara benzena dengan etanoil klorida, CH3COCI
dengan kehadiran aluminium triklorida, AICI3.
(1) Draw the structural formula of compounds X, Y, and z.
Lukiskan formula struktur bagi sebatian X, Y, dan Z.
(ii) Show the formation of electrophile that will be reacted with benzene…
What is the structure of the principal organic product formed in the reaction of 1-iodopropane with NaSH?
Chapter 9 Solutions
EBK EXPERIMENTAL ORGANIC CHEMISTRY: A M
Ch. 9.2 - Prob. 1ECh. 9.2 - Prob. 2ECh. 9.2 - Prob. 3ECh. 9.2 - Prob. 4ECh. 9.2 - Prob. 5ECh. 9.2 - Prob. 6ECh. 9.2 - Prob. 7ECh. 9.2 - Prob. 8ECh. 9.2 - Prob. 9ECh. 9.2 - Prob. 10E
Ch. 9.2 - Prob. 11ECh. 9.2 - Prob. 12ECh. 9.2 - Prob. 13ECh. 9.2 - Prob. 14ECh. 9.2 - Prob. 15ECh. 9.2 - Prob. 16ECh. 9.2 - Prob. 17ECh. 9.2 - Prob. 18ECh. 9.2 - Prob. 19ECh. 9.2 - Prob. 20ECh. 9.2 - Prob. 21ECh. 9.2 - Prob. 22ECh. 9.2 - Prob. 23ECh. 9.2 - Prob. 24ECh. 9.3 - Prob. 1ECh. 9.3 - Prob. 2ECh. 9.3 - Prob. 3ECh. 9.3 - Prob. 4ECh. 9.3 - Prob. 5ECh. 9.3 - Prob. 6ECh. 9.3 - Prob. 7ECh. 9.3 - Prob. 8ECh. 9.3 - Prob. 9ECh. 9.3 - Prob. 10ECh. 9.3 - Prob. 11ECh. 9.3 - Prob. 12ECh. 9.3 - Prob. 13ECh. 9.3 - Prob. 14E
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- Assuming you are a chemist and you need to extract ethanolic acid in a benzene solution. Propose and briefly discuss how to extract the ethanolic acid in the benzene solution. Include the reactions involved in each step, if any.arrow_forwardOzonolysis process was carried out towards an unknown organic compound, X, to produce propanal, C3H6O and compound Y. Propanal was then further oxidized into compound Z, C3H6O2 by using potassium permanganate, KMnO4 under acidic condition and heating. As an alternative, compound Y can be produced from the reaction of benzene with ethanoyl chloride, CH3COCl with the presence of aluminium trichloride, AlCl3. (i) Draw the structural formula of compounds X, Y, and Z (ii) Show the formation of electrophile that will be reacted with benzene for the formation of compound Y. (iii) What is the name of reaction to convert benzene into compound Y?arrow_forward(b) Explain the possible reagents for the following chemical reactions. I. 2. II. 1. `OH 2.arrow_forward
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