2.7,New Tab(32,367 unread)- chr xde Encrypted Message E X6 Form 3817YouTube101 Chem101A https://app.101edu.coQuestion 2 of 20Copper(II) phthalocyanine (Cu(Cs2HiGNs)) is produced by thecyclotetramerization of phthalonitrile (CsH&N2) according to thefollowing reaction:C&H&N2(1) + CUCI:(s)Cu(C32H16N:)(s) + Cl:(g)How many moles of copper(II) phthalocyanine would be produced bythe complete cyclotetramerization of 555 grams of phthalonitrile in thepresence of excess copper(I) chloride?| mol3.458.K.34

Balanced reaction of phthalonitrile with CuCl2 4C8H4N2(l) + CuCl2(s) ...> Cu(C32H16N8)(s) + Cl2…

Answered: -> A https://app.101edu.co Question 2…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter22: Reactions Of Benzene And Its Derivatives

Section: Chapter Questions

Problem 22.51P

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Compound K, L and M are three isomers with the molecular formula C5H10O.Compound K cannot be oxidized, while compound M and L can be oxidized.Oxidation of compound L with hot acidified potassium permanganate,KMnO4 solution yields 2-methylbutanoic acid. When treated with Iodoformreagent, yellow precipitation only occurs in compound K. Fehling test onlyyielded positive results for compound L and negative for compound M andK. Compound M is then reacted with hydrogen chloride, HCl produceschlorocyclopentane (i) Draw the structural formula of compounds K, L and M.
Compound K, L and M are three isomers with the molecular formula C5H10O.Compound K cannot be oxidized, while compound M and L can be oxidized.Oxidation of compound L with hot acidified potassium permanganate,KMnO4 solution yields 2-methylbutanoic acid. When treated with Iodoformreagent, yellow precipitation only occurs in compound K. Fehling test onlyyielded positive results for compound L and negative for compound M andK. Compound M is then reacted with hydrogen chloride, HCl produceschlorocyclopentane. (ii) Name the type of chemical reaction of compound M when reacted withhydrogen chloride, HCl .
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Data: Density of p-phenetidine is 1.065g/mol Williamson Ether Synthesis: Mass of filter paper: 0.680 g Mass of filter paper and product: 1.482 g Melting Point: 134-136oC Amide Synthesis: Mass of filter paper: 0.686 g Mass of filter paper and product: 1.589 g Melting Point: 135-137oC Mixed Melting Point (product of amide synthesis mixed with Williamson Ether synthesis product): 134-136oC (a)Calculate theoretical yield of both williamson ether synthesis of phenacetine and amide synthesis of phenacetin. (b) calculate the percent yield of phenacetin obtained via williamson ether synthesis. (c) Calculate the percent yeild of phenacetin obtained via the amide synthesis.
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