C357_Final_Exam_A_2004_comp

C357_Final_Exam_A_2004_comp - Cornell University Chemistry...

Info icon This preview shows pages 1–5. Sign up to view the full content.

View Full Document Right Arrow Icon
Cornell University Chemistry 357 Summer 2004 Final Examination July 02, 2004 Instructions: Read all questions completely before answering. If the question is still unclear, be sure to ask for clarification. You may find it helpful to first answer those questions that you find easier and then return to those you find more difficult. Good Luck!!! Possible Problem Score 1 20 3 25 4 5 6 7 8 9 10 30 16 20 25 25 16 2 25 16 11 12 14 13 12 30 30 30 TOTAL 400 15 30 30 16 17 30 Name:_____________________________________________ Signature:__________________________________________
Image of page 1

Info iconThis preview has intentionally blurred sections. Sign up to view the full version.

View Full Document Right Arrow Icon
Page 1 of 14 1) (20) Provide IUPAC names for each of the following structures and write your answer on the line to the right of the structure. Be sure to include any appropriate stereochemical designations. a) b) c) d) e) H 3 C H H H H 3 C CH 3 H CH 3 Br CH 3 Br H CH 3 H H CH 3 H 3 C H
Image of page 2
Page 2 of 14 2) (25) The following bimolecular reaction can produce 5 products with the chirality shown, in addition to relationships with the other products. Draw the correct products in the boxes shown. OH Br H H H NaOH, H 2 O Chiral Chiral Achiral Achiral Achiral Product A Product B Product C Product D Product E R e l a t i o n s h i p s A and B are structural isomers B and D are structural isomers B and E are structural isomers A and E are structural isomers A and D are structural isomers D and E are diastereomers C has no relationship to A, B, D, or E
Image of page 3

Info iconThis preview has intentionally blurred sections. Sign up to view the full version.

View Full Document Right Arrow Icon
Page 3 of 14 3) (25) In the molecule whose structure is given below, encircle and identify the following: a. a sigma bond b. a pi bond c. atom using sp3 hybrid orbitals d. atom using sp2 hybrid orbitals e. atom using sp hybrid orbitals f.
Image of page 4
Image of page 5
This is the end of the preview. Sign up to access the rest of the document.

{[ snackBarMessage ]}

What students are saying

  • Left Quote Icon

    As a current student on this bumpy collegiate pathway, I stumbled upon Course Hero, where I can find study resources for nearly all my courses, get online help from tutors 24/7, and even share my old projects, papers, and lecture notes with other students.

    Student Picture

    Kiran Temple University Fox School of Business ‘17, Course Hero Intern

  • Left Quote Icon

    I cannot even describe how much Course Hero helped me this summer. It’s truly become something I can always rely on and help me. In the end, I was not only able to survive summer classes, but I was able to thrive thanks to Course Hero.

    Student Picture

    Dana University of Pennsylvania ‘17, Course Hero Intern

  • Left Quote Icon

    The ability to access any university’s resources through Course Hero proved invaluable in my case. I was behind on Tulane coursework and actually used UCLA’s materials to help me move forward and get everything together on time.

    Student Picture

    Jill Tulane University ‘16, Course Hero Intern