CHEM 210 Lecture Notes - Lecture 4: New Zealand Am Class Electric Multiple Unit

Updated Substitutions and Eliminations 2 Pool Points-35 Points Due Wednesday November 1, before class. Please only hand in this sheet, printed double sided. (22 points) In the followin indicate the predominant mechanism (SN1, SN2, E1 or E2) of each reaction. 1) e table, draw the major and any minor products of the reactions shown and Product Reaction Type Starting Material Conditions KOtBu a) (CHICOH, 82℃ b) CH3OH, 0℃ NaSCH(CH3)2 DMF, O'C CH OH o C DBU,DMF NaCl CI c) d) e) H20 22℃ NaNg g) h) NH2Me 22℃ NaOCH3 CH3OH, 40 C NaOCHs k) ochち CHOH, 40 Page 1 of 2

..1 Sprint令 9:16 AM @ * 100% X CHEM 242QUIZ17S201...l QUIZ CH. NAME CHEM 242 17 Mar. 2, 2018 (Friday) Score:_ *Please write every resonance structure of the intermediate of the following reaction and explain which isomer would the major product. 1.(5) Aniline + HNO,/H,SO, à 2.(5) Please write the reaction scheme for the synthesis of the following compounds from benzene, m- Nitropropylbenxene

ORGANIC CHEMISTRY 1-CHEM 210-01 (Fall 2017) nstructor: Dr.Young-Gi Kim Department of Chemistry, Delaware State University ORGANIC CHEMISTRY I Lecture CHEM 210-01 (Fall 2017) Chapter Quiz Ch.1 (20 pts/10 Question)/ Date: (1-3) Draw Lewis structures for the following compounds 1. ammonia, NHs DR: 2. Ethyl alcohol, C2HsOH 3. dimethylamine, CH3NHCH3 4. Give the molecular formula for the following compound. 5. What is the bond angle of sp hybridization (6-7) Write electronic configurations of the following elements and the number of valent electrons. 6.C 7. F 8. What is the covalent bonding? Define it. 9 How many electrons are contained between two nuclei in the case of double bond? 10. Draw the common bonding patterns of the following atoms in neutral condition in organic compounds and ions a. C b. N c. O d. F