CHEOrganicChemistryI

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1、62CHE-310 Organic Chemistry IInstructor: Dr. James L. LyleOffice: NSM-D-323Phone: (310) 243-3388; 243-3376Office Hours: Will be announced in class; open door policye-mail:jlylecsudh.edu1. Grading:Daily exams = 1004 exams 100 pts = 400 final exam = 100 homework required 600Letter grades will be assig

2、ned on the following basis. Grades are not curved.A = 100-93%, A- = 92-90%, B+ = 89-87%, B = 86-83%, B- = 82-80%,C+ = 79-77%, C = 76-73%, C- = 72-70%, D+ = 69-67%, D = 66-60%,F = 59-0%2. Required Texts: Organic Chemistry, 6th Ed., Morrison & Boyd. Study Guide for . Molecular Model Kit Supplement.3.

3、Exams.Daily exams will be given at the beginning of most lectures. No make up exams will be given, but the two lowest will be dropped. Attendance is expected. If you miss a daily exam it will count toward one of the two dropped exams. For scheduled hourly exams, no make up exams will be given. You m

4、ust take the exams on the dates and times as scheduled.4. Final exam.The final exam will be comprehensive.5. Homework.Daily homework will be assigned. It is due at the beginning of the following lecture period. Penalty points will be assigned for missing or late homework.6. Prerequisites.The prerequ

5、isite for this course is completion of both semesters of General Chemistry. A corequisite is enrolment in CHE-311.7. Office Hours.The instructor is available at any time outside of class for questions, etc. Do not hesitate to seek help if you need it.8. Cheating. Dont do it! At best you will receive

6、 a failing grade and be put on academic probation, at worst you will be expelled from the university. Review the University Catalog statement on Academic Integrity!9. Course goals, objectives and requirements are covered in the rest of this syllabus.CHE-310TENTATIVE SCHEDULEFall 02MeetingDateChapt.T

7、opic 1.8/26 1Introduction/Basic Principles 2.8/28 1Basic Principles 3.8/30 1Basic Prinicples 9/2no class 4.9/4 2Methane 5.9/6 2Methane 6.9/9 2Methane/Alkanes 7.9/11 3Alkanes 8.9/13 3Alkanes 9.9/16 3Alkanes10.9/18* EXAM I *11. 9/20 4Stereochemistry12.9/23 4Stereochemistry13.9/25 4Stereochemistry14. 9

8、/27 5Alkyl Halides15.9/30 5 Alkyl Halides16.10/2 5/7Alkyl Halides17.10/4 6Alcohols18.10/7 6Alcohols/Ethers19.10/9 6Ethers20.10/11* EXAM II *21.10/14 8Alkenes, synthesis22.10/16 8Alkenes, synthesis23.10/18 9Alkenes, reactions24.10/21 9Alkenes, reactions25.10/23 9Alkenes, reactions26.10/25 9Alkenes, r

9、eactions27.10/28 10Stereochemistry28.10/30 11Dienes29.11/1 11Dienes30.11/4 12 Alkynes31.11/6 * EXAM III *32.11/8 13Alicyclics33.11/11 13Alicyclics34.11/13 13Epoxides35.11/15 14Aromatic Hydrocarbons/Benzene36.11/18 15Electrophilic Aromatic Substitution37.11/20 15Electrophilic Aromatic Substitution38.

10、11/22 15Electrophilic Aromatic Substitution39.11/25 16Arenes40.12/27 16Arenes11/29no class, Thanksgiving holiday41.12/2 16Arenes42.12/4 * EXAM IV *43.12/6TBA44.TBA* FINAL EXAM *CHEM-310 Information re Exam IIn studying for your first exam in this course, you should first go over all of the homework

11、assignments and make sure that you understand them. In fact, you should be able to do any of the assigned homework problems on the exam. This is more difficult than doing the homework when you have access to your notes, etc. One way to prepare would be to redo all of your homework as if it were an e

12、xam. Then, pay particular attention to those problems that you cannot do or do not understand. If you have questions about any of the assigned material you should seek help immediately.- be able to define important terms.- from atomic numbers be able to give the numbers of protons and electrons in a

13、 neutral atom.- be able to give spectral notations for neutral atoms.- be able to identify ionic and covalent bonding.- be able to draw Lewis dot structures for simple molecules.- state the types of hybrid orbitals used in simple molecules and give their angles.- know the relative strengths of some

14、simple acids and bases.- for acid base reactions, be able to predict if a reaction takes place, or if the reaction is given, label the stronger and weaker acids and bases.- be able to predict which compounds are polar.- predict the important products of the reactions of methane.- be able to name alkanes.- know the mechanism

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