Solution :
The formation of two reaction intermediates having more stable product B is given below.
draw a reaction energy diagram. compound A is converted into a more stable product B upon...
9. Draw an energy diagram f formation of i-bromopentane product and another curve on the same diagram show the formation of bromopentane product. Label the positions for all reactants, intermediates, and products.W or the addition of HBr to l-pentene. Let one curve on your diagram show the 2- the higher-energy carbocation intermediate? Which curve has the higher-e nergy first transition state? 9. Draw an energy diagram f formation of i-bromopentane product and another curve on the same diagram show the...
12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Brz and draw an energy diagram for both products. Show both products on the same graph with energy on the Y axis and reaction coordinates on the X axis. (4 points) Br2 ether buta-1,3-diene 11. Show the product and use arrows to show the mechanism for the Nucleophilic Aromatic Substitution Reaction below. Assume benzyne is an intermediate. Just write B: to represent a strong base reacting...
heat two products HBr ether 4- KMnO4 H30 9. Carry out the transformation below. More than one step will be required. Use any reagents you need. Show all reagents and intermediate structures. (4 points) -OH Br 12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Brz and draw an energy diagram for both products. Show both products on the same graph with energy on the Y axis and reaction coordinates on the X axis. (4...
Also Draw Product A and B Consider the reaction of 2-methyl-1,3-cyclohexadiene with HCl Intermediate A Intermediate B НCІ (Less stable resonance form) (More stable resonance form) CIT CI Product B Product A Assuming that the reaction takes place at a very low temperature, draw the intermediate and product structures, including any formal charges. Draw intermediate A Draw intermediate B Rings Select Draw More Select Draw Rings More Erase Erase Cl C н C н
For the following reaction draw in the a) reagents and curly arrows needed as well as the products b) draw in the carbocation leading to the respective product in the energy diagram below. c) Explain why the major product forms to a greater degree based upon the reaction coordinate diagram. 1. less substituted carbocation more substituted carbocation Lower Activation Energy Ea
Draw a structural formula for the more stable cabection mediate formed in the reaction shown CH, H2C=CHCH,CHCH2 + HI . You do not have to consider stereochemistry . Do not include anionic countersons, E.T. in your answer • For cases in which carbocations of the same or Sumilar stability are expected Draw a structural formula for the map o n product of the reaction shown wall of the true сн. H2CCHCH,CCH3 + HBr сн. its2reg • You do not have...
I need help on all of these please 1. Draw the energy diagram that correctly depicts the following reaction (AG<0) and the transition state for the rate determining step. Label substrate (S), product (P), and intermediate (1) if applicable. OTS + NaBr TsONa polar aprotic solvent transition state free energy reaction progress 2. Complete the following reaction schemes. CH3OH 0°C alkyl halide nucleophile ТА polar aprotic solvent 3. Compound A and B are constitutional isomers with molecular formula C5H11Br. When...
draw a mechanism for the following reaction. Draw one additional alkene product and indicate if it is more or less favoured than the one shown. 7. Draw a mechanism that accounts for the formation of the following two products. i) Draw one additional alkene product and indicate if it is more or less favoured than the one shown.
6. Draw a i) mechanism and ii) an energy profile diagram for the following Sn1 reaction? [9] B OH
Consider the serine protease, chymotrypsin. Draw the energy diagram of the reaction catalyzed by chymotrypsin and label all relevant points (intermediates, transition states, reactants, products) a. Draw a dipeptide as a general substrate for chymotrypsin, and draw out the mechanism (use arrows!) describing the proteolytic reaction from the beginning until the covalent intermediate (not the tetrahedral intermediate). b.