1. Give IUPAC names fro the following alkyl halides:(a) CH3CH2CH2CH2I(blCH3(c)CH3CH3CHCH2CH2CIBrCH2CH2CH,CCH2BrCH3Į CH,CH2CICH3CHCHCH,CH3(d)CH3le)(d)BrCH3CCH2CH2CICH3CHCH2CH2CHCH3ČI2. Give the equivalent systematic names of the common names in C.1.

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Answered: 1. Give IUPА names fro the following…

1. Give IUPА names fro the following alkyl halides: (a) CH3CH2CH2CH2I (bl CH3 (c) CH3 CH3CHCH2CH2CI BrCH2CH;CH;ċCH,8r CH3

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Concept explainers

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.

Question

1. Give IUPAC names fro the following alkyl halides:
(a) CH3CH2CH2CH2I
(bl
CH3
(c)
CH3
CH3CHCH2CH2CI
BrCH2CH2CH,CCH2Br
CH3
Į CH,CH2CI
CH3CHCHCH,CH3
(d)
CH3
le)
(d)
Br
CH3CCH2CH2CI
CH3CHCH2CH2CHCH3
ČI
2. Give the equivalent systematic names of the common names in C.1.

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