{[ promptMessage ]}

Bookmark it

{[ promptMessage ]}

CH310M-POW-1_KEY - POW-1 Williams 310/318M Due Date NOON...

Info icon This preview shows pages 1–4. Sign up to view the full content.

View Full Document Right Arrow Icon
POW-1 Williams 310/318M Due Date, NOON Tues, 9/7/10 Name (print): ___________________________________________________________ Signature: ______________________________________________________________ Please write the first three letters of your last name in the boxes
Image of page 1

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

View Full Document Right Arrow Icon
POW-1 Williams 310/318M Due Date, NOON Tues, 9/7/10 1. Lidocaine (pictured below) was introduced to the commercial market in 1948, and quickly became one of the most widely used local anesthetics. Describe each highlighted bond (a e) in terms of the overlap of atomic orbitals. (If there is a double bond, then identify the orbitals that form both the sigma and pi bonds). (1 pt) a.) sp2-sp3 d.) sp2-sp2, 2p-2p b.) sp2-sp2, 2p-2p e.) sp3=-sp3 c.) sp2-sp2 CH 3 CH 3 H N O N CH 3 CH 3 Lidocaine a. b. c. d. e.
Image of page 2
POW-1 Williams 310/318M Due Date, NOON Tues, 9/7/10 2. Shown below is benzyl anion, a relatively stable anion due to resonance delocalization. Draw the other significant resonance structures. Be sure to indicate the flow of electrons through the use of curved arrows (push the electrons!) and don’t forget the charge. (3 pt) 3. Draw the structural formula for the following compounds based on their IUPAC name. (2 pt)
Image of page 3

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

View Full Document Right Arrow Icon
Image of page 4
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