For the chlorination of propane, the two isomers shown here arepossible.CH;CH;CH, + Cl,ÇICH;-CH,-CH,-d + CH;-CH-CH;1-chloropropane2-chloropropanePropane has six hydrogen atoms on terminal carbon atoms-called primary (1°) hydrogen atoms-and two hydrogen atoms onthe interior carbon atom-called secondary (2) hydrogen atoms.a. If the two different types of hydrogen atoms were equallyreactive, what ratio of 1-chloropropane to 2-chloropropanewould we expect as monochlorination products?b. The result of a reaction yields 55% 2-chloropropane and 45%1-chloropropane. What can we conclude about the relativereactivity of the two different kinds of hydrogen atoms?Determine a ratio of the reactivity of one type of hydrogenatom to the other.

If the reactivity is equal then the expected yield ratio of 1-chloropropane to 2-chloropropane is;…

Answered: For the chlorination of propane, the…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL2: Mass Spectrometry

Section: Chapter Questions

Problem 20CTQ

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• -- H (b) H,C 3-methylhexane CH, (c) B கூ CH, CH, HgCG; சீகூ H₂CH H 3-ethyl-1-methyloctane 3,3 diethyl pentane 5Å, Å,CH, W CH3 CH2 CH₂ W21 Su2... CH3 X -CH3 G b F E L c
1. Write condensed structural formula for all isomers of compounds that fulfill the following requirements: (a) Alkenes with molecular formula CsH10. (b) Alkynes with molecular formula C4H6. (c) Dienes with molecular formula C4H6. 2. For each of the following, give the order of increasing boiling point: (a) n-Heptane, n-octane and n-hexane. (b) n-Pentane, isopentane and n-hexane. (c) 2-Methylhexane, n-heptane and 3,3-dimethylpentane. 9 3. Isomeric compounds can sometimes be distinguished by observing the number of mono- brominated compounds that each forms. In the following cases decide which isomer is present by the number of compounds that are formed. (a) Compound A forms four monobromo compounds. Is it 2-methylbutane or n-pentane? (b) CompoundB forms four monobromo compounds. Is it 2- methylpentane or 3- methylpentane? (c) Compounds C forms monobromo compound. Is it cyclopentane or one mehtylcyclopentane? 4. A hydrocarbon C5H12 was allowed to react with bromine. Only monobromo…
Draw the structure of cis-1,2-dimethylcyclohexane. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • You do not have to explicitly draw H atoms. opy aste
Draw the structures of 1,3-pentadiene and 1,4-pentadiene and label the carbons. Predict the trendin C-C single bond lengths in the two compounds.
Name these organic compounds: structure name CH3 CH,=C– CH; CH3 CH,- CH– CE CH CH, CH, — CH, — с — СH, I Don't Know Submit Terms of O 2021 McGraw Hill LLC. All Rights Reserved. MacBook Air
Draw the structure of cis-1,2-dimethylcyclohexane. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • You do not have to explicitly draw H atoms.
11. Compound X, (CH3)2CHCN, can be formed from a haloalkane, C3H7Br.(i) Name compound X............................................................................................................................(ii) Give the reagent and conditions necessary to form X from C3H7Br.Reagent..............................................................................................................Conditions..........................................................................................................(iii) Name and outline the mechanism for this reaction, showing clearly the structure of C3H7Br.Name of mechanism..........................................................................................Mechanism.
The meiting points and boiling points of two isomeric alkanes are as follows: CH3(CH2);CH3, mp = -57 °C and bp = 126 °C; (CHalsCC(CH3)3, mp = 102 °C and bp = 106 °C. (a) Explain why one isomer has a lower melting point but higher boiling point. (b) Explain why there is a small difference in the boiling points of the two compounds, but a huge difference in their melting points.
From the data in Figure 4-12 and Table 4-1, estimate the percentages of molecules that have their substituents in an axial orientation for the following compounds: (a) Isopropylcyclohexane (b) Fluorocyclohexane (c) Cyclohexanecarbonitrile, C6H11CN
- compound CH₂ 1 CH, CH-CH₂-CH₂ CH, CH₂ | | CH₂-CCH₂ CH₂ CH₂ I CH₂CH₂ - CH, I CH₂ I CH₂CH₂-CH-CH₂ - CH₂ name 2-methylbutane 3-ethylpentane
An alkene forms 2-methylbutane when catalytically reduced and 2,3- dibromo-2-methylbutane when treated with Br₂. Draw the structural formula of the alkene. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. . In cases where there is more than one answer, just draw one. / 8 MULL / #[ ] در O- √n ?
1. Which of the following formulae represent the same compound? (1) CH;CH,CH;CHCH3 (3) CH-CНCH, 1. CH2 (2) CH3 CH3 CHCH;CH2 CH3 CH3 CH;CH3 (4) CH;CHCH,CH,CH3 (5) CH;CH,CHCH;CH3 CH3 CH3 A. (2) and (3) only В. (1), (2) and (4) only С. (1), (4) and (5) only D. (1), (2), (3) and (4) only

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