For the following reaction draw in the a) reagents and curly arrows needed as well as...
Input curly arrows to present the reaction of a carbonyl with mineral base and mineral acid, and write the ionic product of each reaction. HCI Cl NaOH Na OH a. Neutral water will react with a carbonyl. Tor F. b. Neutral water will react with a carbonyl upon carbonyl acidification activation catalysis. T or F C. Show carbonyl activation of contributor #1 using curly arrows. Show the conversion of contributor #1 into contributor #2 using curly arrows as well. d....
HH on. Draw the mechanism, including curly arrows, 11. Consider the following reaction. Draw the mechanism, including curl that shows why one product is major and the other is minor OH HC-C-CH2-CHE H2SO4 H₂C CH3 -H₂O c=CH-CH3 + H2C=C-CH2-CHg H₂C CH3 MAJOR MINOR
Draw the final product(s) and show using curly arrows the mechanisms for the following reaction. CH3
For the reaction coordinate diagram shown below, which of the following statements are true? Energy Reaction Coordinate True AErxn = A-C True Reaction is endothermic False Ea(forward) = Ea(reverse) True A represents the energy of the starting materials False Ea(forward) = B-C True Eg of the forward reaction is less than Ea of the reverse reaction Remember that thermodynamic quantities are calculated by products - reactants. The activation energy can be thought of as the barrier height.
6) Draw the structure of (Z)-1-chloro-2-methyl-2-butene. 7) Draw the curved arrows to show how CH3CH=CHCH2CH3 reacts with HBr to form a carbocation first, and then forms 2-bromopentane. (this is 2 steps) 7) 8) 8) Predict the product(s) of the following reaction based on the curved arrows: Make sure to include + and- charges where appropriate. -C-NH2 CH CHy HO 9) Based on the following reaction coordinate diagram: Which compound, A or C, is formed faster from B? Which is more...
8. Draw an arrow-pushing mechanism to show the alkene isomerization from to B CH3 cat. H3O* A B A Draw the reaction coordinate diagram for the reaction above from A to B. reaction coordinate Regardless of the ratio of A to B at equilibrium, when the above transformation is run dilute in H2O at lower temperature, another product forms as the major product. Draw that product below. Free Enely 8. Draw an arrow-pushing mechanism to show the alkene isomerization from...
CH3 7) Draw in the appropriate curly arrows for the following El mechanism. Note! The below steps are the steps in a single mechanism for a single reaction! Pay attention to lone pairs (i.e. draw them in if appropriate.) Also write in hidden hydrogens that are in the vicinity of the reaction site. HO Start by rewriting each of the reactants. Then use "arrow pushing" to show how the reactants are converted to products, assuming an El mechanism. Be sure...
Let's continue on the rates of reactions diagrams & reaction coordinate 3. Here is a reaction energy diagram. Label the poolo transition state м2 терге TH reactants products 1345 in NLB Reaction Coordinate graph, please draw & label both the activation energy (Ea! overall energy change for the reaction CAE). . On the & the Toensuz gopstod reactants ولدانهم Reaction Coordinate
T ylic uelydration reaction, draw the curved arrow mechanism leading to the major alkene product and one of the minor alkene products. Draw a picture of the hyperconjugation interaction that explains the greater thermodynamic stability of the major product versus the minor product. Concisely explain why the uncatalyzed dehydration reaction would not form the carbocation intermediate Me catalytic H2SO4 -он H,0
8, Draw the reaction coordinate, label appropriate points (i.e., reaction energy, activation energy ), and draw the three possible products for the bromination of tert-butoxvbeazene, Make sure to include the three reaction pathways for the formation of the three different isomers that can form. Indicate the major and minor products 8, Draw the reaction coordinate, label appropriate points (i.e., reaction energy, activation energy ), and draw the three possible products for the bromination of tert-butoxvbeazene, Make sure to include the...