propose a synthetic route to this structure that includes at least one C-C bond formation step.

Predict Products. Using line structures, give the major product of each 1.[ reaction below. DON'T SHOW MECHANISMS HERE. Use scratch paper if needed. H2 a) Pt/C b) HBr H2SO4 HO

Show which position of the 6 aromatic carbon is (are) the most electron rich by drawing detailed resonance delocalization with curved arrows. Conclude whether the molecule is ortho/para or meta director Predict the product of the following reaction and draw a detailed mechanism. Draw curved arrow to show the mechanism. Show two resonance structures for the intermediate. OCH 3 HNO3 H₂SO4

Major product and mechanism for this reaction?

For the reaction A + B --> 2 C, Kç = 0.16. A 2.00 L flask is filled with 1.00 mol A and 1.00 mol B, and allowed to come to equilibrium. Determine the concentrations, in moles/liter, of A, B and C at equilibrium. (Do not input units, 3 sig figs). A = B = C =

4) Show a detailed mechanism for the following transformation. OH OH OH HO HO -H OH CH₂OH HCI HO HO. OH -H OHI SOCH 3 HO -OCH 3 OHI H

Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps.

Macmillan Learning Use the table of bond dissociation energies to calculate and compare the enthalpy of monobromination and monochlorination for the given alkyl position. Bond Dissociation Energies (for A-B- A+B) Bond broken H-H Br-Br CI-CI CH₂CH₂CH₂-H+ Br₂ CH₂CH₂CH₂-H + Cl₂ AH (kJ/mol) Bond broken AH (kJ/mol) 436 366 193 432 243 H-Br H-Cl CH₂CH₂CH₂-Br + HBr CH₂CH₂CH₂-CI+HCI Bond broken AH (kJ/mol) CH₂CH₂CH₂-H 423 CH₂CH₂CH₂-Br 294 CH₂CH₂CH₂-CI 354 AH = ΔΗ = -58 Incorrect -131 Incorrect kJ/mol kJ/mol