3. (a) (4 pts) Draw the thermodynamic and kinetic products of the hydrolysis of 3-bromo-3- methylbut-1-ene,...
Draw the mechanism for the production of 1 major product of the following reactions. 1) 2-methylbut-2-ene reacted with hydrochloric acid. 2) (Z)-3-methylpent-2-ene reacted with bromine.
In the lab, Cassandra the Chemist™ studied the reaction between 2-bromo-3-methyl pentane with a base under the presence of heat. During her studies, she found that the reaction rate doubled when she doubled the amount of the base. Draw a full, arrow-pushing, mechanism of the above reaction showing the most prevalent product formed. 11. (22 pts) In the lab, Cassandra the Chemist"M pentane with a base under the presence of heat. During her studies, she found that the reaction studied...
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH),CBr + 24,0 → (CH),COH + H20* + Br Give the Sn1 mechanism. Draw structures - including electrons and charges - and add curved arrows. Details count. Step 1 - Draw 2-bromo-2-methylpropane - Add one curved arrow. Draw the step 1 products: 1 organic species; 1 inorganic species. Map Step 2 . Reproduce the organic product of step 1. - Add one curved arrow to show water reacting with the organic species. Draw...
7-9 please! 4 7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) H Acidity of one pf the H's shown H H 8. For the reaction show a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control" product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures...
please help me by answeing part 2. please include mechanism. Electrophilic addition of HBr to 3-methylbut-1-ene gives a mixture of two constitutional isomers. Only one of the isomers, however, is formed when the 2 methylbut 2 ene reacts with HBr in the presence of peroxides. Draw each of the isomers. Part 1: Draw the isomer that is formed in both reactions Br view structure Part 2 out of 2 Draw the isomer formed only in electrophilic addition reaction. edit structure......
7. (4 pts.) In Figure 3 of Section 4 “Designing the Drug Thalidomide”, two possible hydrolysis products are shown. Provide the mechanism to generate compound 4. The first step of the mechanism with the curved arrow pushing is done for you. O + H-OH2 -N: Н. 0:0:- -NH2 N- 4 -ОН о о
Using 3 different sets of reagents on 3-methylbut-1-ene, it s possible to obtain 3 different alcohols. Specify which reagent will produce the indicated alcohol from 3-methylbut-1-ene QUESTION 1 Match the reagent to the specified outcome | ??? 3-methylbut-1-ene A. Not possible in one step 니 H₂SO4, Ho 3-methylbutan-2-ol 1. Hg(OAc)2, H2O) 2. NaBH4 \ 1. BH3: THE 3-methylbutan-1-ol 2. NaOH, H2O, HO 2-methylbutan-2-ol HOT 2-methylbutan-1-ol
1. Draw the mechanism (arrow pushing) of the reversion of tert-pentyl chloride (the product) to tertpentanol (the starting material) 2. Draw the mechanism of the conversion of tert-pentanol (the starting material) to 2-methylbut-2- ene
7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) Acidity of one pf the it's shown 8. For the reaction show, a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures for the intermediate (4 pts) Br...
19. Which are the kinetic products in the energy diagram below, and which are the thermodynamic products? Explain. 20. Which atom (s) is/are the electrophilic site(s) in the structure shown below: 21. Identify the arrow-pushing pattern that is being utilized in the mechanism shown below. Explain. gege- &