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Course: CHEM 236, Spring 2011
School: UIllinois
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Spectroscopy IR Slides for Notes Wednesday, March 30, 2011 and Friday, April 1, 2011 chloroform chloroform-d hexane 1-hexene 1-hexene 3-hexene 1-hexene 1-hexyne 1-hexyne 2-hexyne hexane 1-hexanol 1-hexanol 1-hexylamine 1-hexanol hexanal hexanal 2-hexanone hexanal methyl hexanoate methyl hexanoate hexanoic acid

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Spectroscopy IR Slides for Notes Wednesday, March 30, 2011 and Friday, April 1, 2011 chloroform chloroform-d hexane 1-hexene 1-hexene 3-hexene 1-hexene 1-hexyne 1-hexyne 2-hexyne hexane 1-hexanol 1-hexanol 1-hexylamine 1-hexanol hexanal hexanal 2-hexanone hexanal methyl hexanoate methyl hexanoate hexanoic acid
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UIllinois - CHEM - 236
CHEMISTRY 236ORGANIC CHEMISTRYResonance HybridsMolecules which are not adequately represented by a single Lewis structure areoften described as a hybrid of two or more Lewis structures. A resonance hybridhas only a single stable structure. However, r
UIllinois - CHEM - 236
SN2Rate=k[alkyl halide][nucleophile]-Best for primary halides-Inversion of configuration-Need good nucleophile-NO intermediateSN1Rate=k[alkyl halide]-Best for tertiary halides-Racemic mixture-Carbocation intermediate (why tertiaryis best!)E2R
UIllinois - CHEM - 236
Due Date: April 13, 2011 1Solutions to Problems: Chapter 13Due Date: April 13, 2011 2Solutions to Problems: Chapter 13Due Date: April 13, 2011 3Solutions to Problems: Chapter 13
UIllinois - CHEM - 236
Due Date: April 6, 2011 1Solutions to Problems Chapter 12Due Date: April 6, 2011 2Solutions to Problems Chapter 12
UIllinois - CHEM - 236
Due Date: April 20, 2011 1Problems to Solutions Chapter 14Due Date: April 20, 2011 2Problems to Solutions Chapter 14
UIllinois - CHEM - 236
Due Date: April 27, 2011 1Solutions to Problems Chapter 15Due Date: April 27, 2011 2Solutions to Problems Chapter 15
UIllinois - CHEM - 236
Due Date: February 2, 2011 1Solutions to Problems Chapters 2 & 4Due Date: February 2, 2011 2Solutions to Problems Chapters 2 & 4Due Date: February 2, 2011 3Solutions to Problems Chapters 2 & 4Due Date: February 2, 2011 4Solutions to Problems Chapte
UIllinois - CHEM - 236
Due Date: February 9, 2011 1Solutions to Problems Chapters 4 & 5Due Date: February 9, 2011 2Solutions to Problems Chapters 4 & 5Due Date: February 9, 2011 3Solutions to Problems Chapters 4 & 5Due Date: February 9, 2011 4Solutions to Problems Chapte
UIllinois - CHEM - 236
Due Date: September 15, 2010 1Solutions to Problems Chapters 5 & 6Due Date: September 15, 2010 2Solutions to Problems Chapters 5 & 6Due Date: September 15, 2010 3Solutions to Problems Chapters 5 & 6Due Date: September 15, 2010 4Solutions to Problem
UIllinois - CHEM - 236
Due Date: February 23, 2011 1Solutions to Problems Chapters 7 & 8Due Date: February 23, 2011 2Solutions to Problems Chapters 7 & 8Due Date: February 23, 2011 3Solutions to Problems Chapters 7 & 8
UIllinois - CHEM - 236
Due Date: January 26, 2011 1Solutions to Problems Chapters 1 & 31.31Due Date: January 26, 2011 2Solutions to Problems Chapters 1 & 3Due Date: January 26, 2011 3Solutions to Problems Chapters 1 & 33.7(a)Due Date: January 26, 2011 4Solutions to Pr
UIllinois - CHEM - 236
Due Date: March 2, 2011 1Soluttions to Problems Chapter 8Due Date: March 2, 2011 2Soluttions to Problems Chapter 8
UIllinois - CHEM - 236
Due Date: March 9, 2011 1Soluttions to Problems Chapter 9Due Date: March 9, 2011 2Soluttions to Problems Chapter 9Due Date: March 9, 2011 3Soluttions to Problems Chapter 9Due Date: March 9, 2011 4Soluttions to Problems Chapter 9
UIllinois - CHEM - 236
Due Date: March 16, 2011 1Solutions to Problems Chapter 10Due Date: March 16, 2011 2Solutions to Problems Chapter 10
UIllinois - CHEM - 236
Due Date: March 30, 2011 1Solutions to Problems Chapter 11Due Date: March 30, 2011 2Solutions to Problems Chapter 11
UIllinois - CHEM - 236
Due Date: May 4, 2011 1Solutions to Problems Chapter 16Due Date: May 4, 2011 2Solutions to Problems Chapter 16Due Date: May 4, 2011 3Solutions to Problems Chapter 16
UIllinois - CHEM - 236
Fall 2009Chemistry 236Hour Exam 3Last Name _First Name _1. _ 15 pts2. _ 12 pts3. _ 30 pts4. _ 28 pts5. _ 15 ptsTotal: _ 100 pts1. (15 pts) Mechanism. Give a structure for intermediate A and a mechanism for theformation of A and B. Is the stere
UIllinois - CHEM - 236
UIllinois - CHEM - 236
First Three Letters of Last NameNAME _Network ID_Section_CHEMISTRY 236SPRING 2010EXAM IIIAPRIL 2, 2010Note: The last page of this exam is a periodic table.123456(24)(10)(18)(10)(23)(15)100CHEM 236 Spring 2010 2Exam III1. [24 points
UIllinois - CHEM - 236
UIllinois - CHEM - 236
UIllinois - CHEM - 236
UIllinois - CHEM - 236
UIllinois - CHEM - 236
UIllinois - CHEM - 236
NAMECHEM 236Review MaterialAD51) Provide a curved arrow mechanism for the following transformation:OHOD ClMeMeDOHMeHOHOHMeD ClOMeC lOMeHDDDD3) Predict the MAJOR product (only) for the following reactions :N O2N O2FeBr 3Br 2
UIllinois - CHEM - 236
UIllinois - CHEM - 236
FirstThreeLettersofLastNameNAME_NetworkID_Section_CHEMISTRY236SPRING2010EXAMIIMARCH5,2010Note:Thelastpageofthisexamisaperiodictable.1234567(4)(12)(9)(16)(15)(14)(30)100CHEM 236 Spring 2010 2Exam II 1.[4points]Provideacorrectnamef
UIllinois - CHEM - 236
FirstThreeLettersofLastNameNAME_NetworkID_Section_CHEMISTRY236SPRING2010EXAMIVAPRIL28,2010Note:Thelastpagesofthisexamareaperiodictable,IRandNMRvalues.12345678(6)(4)(24)(12)(20)(12)(12)(10)100CHEM 236 Spring 2010 2Exam IV 1.[6p
UIllinois - CHEM - 236
First Three Letters of Last NameNAME _Network ID_Section _CHEMISTRY 236SPRING 2010EXAM IFEBRUARY 12, 2010Note: The last page of this exam is a periodic table.1234567(6)(12)(9)(20)(21)(20)(12)100CHEM 236 Spring 2010 2Exam I 1. [6
UIllinois - CHEM - 236
NAME _First Three Letters of Last NameNetwork ID_Section _CHEMISTRY 236FALL 2009EXAM IIOCTOBER 12, 2009Note: The last page of this exam is a periodic table.1 (9)2 (8)3 (9)4 (9)5 (28)6 (12)7 (16)8 (9)100CHEM 236 Fall 2009 2Exam II 1. [9
UIllinois - CHEM - 236
First Three Letters of Last NameNAME _Network ID_CHEMISTRY 236FALL 2010EXAM ISEPTEMBER 10, 2010Note: The last page of this exam is a periodic table.123456(12)(12)(6)(30)(30)(10)100CHEM 236 Fall 2010 2Exam I 1.[12 pts] Draw structur
UIllinois - CHEM - 236
UIllinois - CHEM - 236
Compound 1C8H7OBr(Integrations arein boxes below)CAB223HCompound 2C5H12O(integrationsare in boxesbelow)GDFE21126
UIllinois - CHEM - 236
CHEM 236Quiz 1 8:00 amKEYNAME1) What is the hybridization state on the indicated atoms? (5 points)HOHHHH3 COOC H3H3 CNNCHCH 3C H3sp2sp3sp3ssp2) Provide a curved arrow mechanism and a product structure for the following transformati
UIllinois - CHEM - 236
CHEM 236 Spring 2011Quiz 3 8:00 amNameScore:/201. (5pts) Describe mechanistically why two different epoxide opening products areobtained when treated with base or acid in the presence of methanol.Na OMeOO H OMevs.MeOHOOMeOHMe OHOS N2 st y
UIllinois - CHEM - 236
CHEM 236 Spring 2011Quiz 5 12:30 pmNameKEYScore:20 /201. (6pts) Predict the products from the following reaction sequences:BH1.2O2. H2 O2 , H 2O , N aOH1. n- Bu Li2.BrN a0 , NH 32. (2pts) Draw a curved arrow mechanism for the following rea
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