number of peaks. integral ratios. and splitting patterns for this compound?

pt Draw the geometrical isomer of the cyclic part of the molecule. Draw the optical isomer of the linear part of the molecule. 2. Based on the molecule above, i. ii.

Chrome File Edit View History Bookmarks > C MInbox (1) X Orgo app.101edu.co Orgo-Go X IV) III) II) Profiles Tab 1) B Login - B. X Window Help Alkyne H. X The MO diagram for 1,3-butadiene (CH₂=CHCH=CH₂) is shown below. Provide the correct number of TT electrons this diagram. Aktiv Che X Inorganic 8888 8 8 8 8 8 8 8 8 8 8 8 8 Question 20 of 29 MacBook Pro & Experiments in Cher

Molecule A Molecule B a. Identify the molecules and highlight all electron dense areas with yellow. b. Encircle all functional groups that show pi electron delocalization (resonance). c. Choose a molecule that has the greater ability to undergo molecular stacking with sphingomyelin. Elaborate using the concepts of intermolecular force of attractions.

Use IR spectroscopy techniques to distinguish the following pairs of compounds: a. b. C. NH2 OCH 3 ii ii ii Br -OH

In IR spectroscopy, the energy absorbed by the molecule causes: A. In plane Bending B. Bond Vibration C. Electron Excitation D. Fragmentation O A & O A & D B&C

4. Please show work