Please explain how you got your answer in detail, and why the other answer choices are incorrect. Thank you !
Please explain how you got your answer in detail, and why the other answer choices are...
Please explain how you got your answer in detail, and why the other answer choices are incorrect. Thank you ! 24. Use the reagents below in the proper order to convert cyclohexene to 1,3-cyclohexadiene. You may assume that all steps produce exclusively the major product. The synthesis can be accomplished in fewer than 4 steps. e.g. if you think this can be accomplished using bromine, then bromine and light, and finally refluxing in sulfuric acid, you would write your answer...
Provide the major product(s) for the following reactions: Show Stereochemistry when necessary HBr Br2 CH2Cl2 HBr Br2 ROOR H20 H2O СН,ОН H30* 1) BH3, THE 2) H2O2, NaOH, H2O 1) Hg(O2CCF3)2 CH3OH 2) NaBH4, NaOH 1) Hg(OAc)2, H20, THF 2) NaBH4, NaOH H2 Pd/C
please do 1-6 the reagents are listed to the right. and each regeant needs to be reacted with each alkene substrates on the left. React each of the alkene substrates on the left with each of the reagents on the right If you see fit. provide kinetic and theromdinamic products as well as all possible diastereomere 10}} 8 1) HBr 2) Br2 3) H2O, H+ 4) Br2, H2O 5) O3, PPh 6) HBr, Peroxides 7) Hg(OAc)2, H2O, NaBH4 8) BH3,...
13. (12 pts-4 pts each) Show how you could carry out th how you could carry out the following synthesis reactions by placing the letters corresponding to the appropriate reagents above each ar must be in the correct order to receive full credit. priate reagents above each arrow. The reagents A. HBr, ether B. Br2, CH2Cl2 C. Br2, H2O D. 1. Hg(OAC)2, H2O/THF 2. NaBH4 E. 1. BH3, THF 2. H2O2, OH F. H2SO4, H2O/HgSO4 G. NBS, hy H. H/Pd/C...
Starting from 3-methylhex-1-ene as the substrate at the center of your page, draw a reaction map showing the regiochemical and stereochemical outcome or outcomes for each of the following series of reagents. Name each of your products, including stereochemical designations for any chirality centers that are generated.**Pay attention to the possibility of rearrangement when your mechanism produces a carbocation. A. H2SO4, H2OB. 1. Hg(OAc)2, H2O; 2. NaBH4C. 1. BH3•THF; 2. H2O2, NaOHD. Br2, CCl4E. Br2, H2OF. HBrG. HBr, ROORH. 1. O3; 2. DMSI. H2, Pt
Answer questions A-D please. ONLY ANSWER THE QUESTIONS IF YOU KNOW IT FOR SURE BECAUSE MY MONEY IS BEING WASTED WHEN MY QUESTIONS ARE BEING ANSWERED WRONG. Thank you!!! A.) Below is a summary of alkene reactions. Complete them by providing the missing structures (including stereochemistry wherever it applies). B.) Draw the structure of the carbocation formed during the reaction of the alkene from chart A with HCl. C.) Draw the mechanism of the reaction of Br2 addition. D.) Draw...
Outline the correct reaction sequence that will successfully transform the indicated starting material into the indicated product. Input your answer as uninterrupted sequence of letters. Do not separate the letters by commas, spaces, dashes, or anything else. If you do then the robo-grader will not recognize it as the correct answer. 5 steps A HBr H2SO4 / heat NBS / UV light KO-t-Bu / t-BuOH (for E2) Hg(OAC)2 / H20 then NaBH4 BH3-THF, then NaOH / H2O2 NaNz/DMSO KCN /...
please write the steps needed to get this product. A NaBH4/H:0 S KMnO4 HNO3 H2SO4 K HNO3 H2SO4 B LiAlH4/H:07 T CH3MgBr/H:0* U 1. LDA/ 2. CH Br C Dess-Martin L Nal D CrOz/H:07 M H3PO4 V NaCN E H/Pd N Bry/FeBr3 W NH 0 CH:COCI/AICI: X CH3NH2 P CH:CH-CT/AICI: Y SOCI: F SnCl/H30* 1. Hg(OAc)2, H2O/THF G 2. NaBHA HH2SO4, H2O, HgSO4 1. BH3, THF 2. H2O2, OH Q H3O+/H20 Z CH OH R KOH O CHICHI CH3CH CH:CH-C-OH...
Select the reagents you would use to accomplish the syntheses shown below in no more than the number of steps specified. List the letters of the reagents in the order that they are used; example: fa. Reagents Available a. HBr b. PBr3 C. (CH3CH2CH2CH2)2Culi f. CH31 g. Hg(OAC)2, H2O, THF; then NaBH4 h. Cl2, light d. (CH3)2Culi I. KOH j. NBS (N-bromosuccinimide) e. BH3, THF; then H202, OH - он CH3 Use 2 steps: V - M Use 3 steps:
PLEASE answer ALL parts! NO explanations needed! THANK YOU :) Part IV. (a) Please give the principle organic product(s) of each reaction, please specify stereochemistry if it applies (18 points) H2SO4 HO Heat 1). BH3. THE 2). H2O2, NaOH HBr Peroxide Brz/H20 CH2Cl2 ? t Brz/hv Bigova NaOCH2CH3 CH3CH2OH, 50 °C HBr Heat OH