What is the product of the following reaction? — н ннн н-с-с-С=С + H2O H,SO, Hн Hн ОН ОН ОН ОН What is the major product formed in the following reaction? сна 3 сні H,SO, Heat нас он 86 39 — 42 45 ОН ОН What product is formed in the following reaction? CH3 H3C-C-OH [O] CH3 No Reaction What product forms in the following reaction? 30 > 33 + HBT ✓ 36 Ono reaction 39 Br 42 45 Br...
15 Complete the mechanism for the following Reaction : HH Hн H-C-C-Br HH - Label each pair of compounds below as:
13. Name each of the following compounds [Rh(NH3),C1,]CI trans-NH.[Co(C,0.),(H,0),] Na [Ru(H2O)C1)
EXERCISE Writing Reaction Mechanisms: Acyl Transfer Electron pairs :0: H-o-H CH3 C Erase + Na :0– CH3 :0 - H Write the first step of the reaction mechanism using curved arrows to show electron reorganization. 0 O H3C- + Na OH HO + H-ô-CH 0 - Nat OCH < Recheck Next (1 of 5)
provide a mechanism and account for the fact that the
bond is trans.
yellow product. NO2 o + H3C-NO2 NaOH MeOH, H2O
Complete the mechanism for the following dehydration reaction by adding formal charges and arrows to indicate the movement of electrons. Write the overall equation at the bottom. O: H-Cl : CH3 CI: CH Нас 2) CH CH3 CH3 H3C H3c 3) CI overall equation:
4. The following reaction has a small, positive AG and takes place slowly at room temper H3C-Cl + H-OH - H3C-OH + H-CI (a) The mechanism for the reaction is shown below. Which bond is being broken in the sky step? Which bond is being made? slow Step 1 H3C-Cl + H-OH- - H3C-CH3 + CI endothermic fast Step 2 H3C-OH3 + 1 - H2C-Cl + H-CI exothermic (b) Based on this multi-step mechanism, draw a free energy reaction coordinate...
Draw the structure of 4-fluorocycloheptanol. Predict the product of the reaction below: H,SO + H2O H3C-CH2-CH2 heat Predict the product of the reaction below: OH H,SO H3C-CH2-CH-CH2-CH3 + H2O heat
5. Complete the following synthesis and draw the mechanism of step 5. O Na Step 1 Step 2 Step 3 Na2Cr207, H2SO4, H2O Step 5 HCI, H2O Step 4 Mechanism of Step 5:
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2-chloro-2-methylpropane reacts with water in three steps to yield 2-methylpropan-2-ol. One of these steps is shown below, add curved arrows to the mechanism to indicate the movement of electrons in this step. estion 6 1pt Arrow-pushing Instructions Question 7 1 pt Question 8 Question Question 10 1 pt pt pe...