Please show the detail mechanism and all work. Thank you. What is the product of the...
Please show all work. Thank you! 6. Predict the product of the reaction sequence shown OH OH Он OH Br OsO4 Cн,CH,0" A В CH,CH-он H2O2 OH OH HO HO C D
Please show all work for Number 5: CH3OH and number 3, HF one. Thank you Complete the following reaction and provide forget resonance structures when applicable. a. a detailed arrow-pushing mechanism. Don't HF OH 5. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s) Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. Cl2/H20 Et AV Use the provided template...
Please show work and explain in detail. Thanks 2. 1) Select the reagents needed for the following reaction: a. H2, Pd-C b. HCI c. H2, Lindlar catalyst d. H2O, H2SO4 2) Consider the mechanism for acid-catalyzed hydration of alkenes. Select the intermediate(s) for the following reaction: H20, H2SO4 nyo yo'n M OH 3) Consider the mechanism for the halogenation of alkenes. Select the intermediate(s) for the following reaction: Br2 JBr + ...Br Br Br Br 11Br VuBr
Only using E1 and E2 and please show mechanism. Thank you. Determine the major elimination product(s) for each of the following reactions. addition, please state the mechanism that is employed in the formation product. (12 points) HO H2SO4 Br NaOC(CH3)3 CH3OH CH3OH Heat
Please show the mechanism showing all possible substitution products. SN1 and SN2 only. Thank you. Determine the major substitution product(s) for each of the following reactions. In addition, please state the mechanism that is employed in the formation of each product. (8 points) Br NaOCH 3 CH3OH H20 Heat
please show all steps including each mechanism (arrows) and also if SN1 has any rearrangements of carbocation intermediate through a hydride shift and/or methyl shift. DO NOT NEED ELIMINATION. ONLY SUBSTITUTION. Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
show all work please thank you!!! 3. (10 pts total) Consider the following alkene addition reaction: Brz H2O НО Br a. (3 pts) This type of alkene addition reaction is mediated by both Lewis acids and bases. Of the two inorganic reactants (Br2 and H2O), place a triangle (1) around the one which functions as a Lewis acid in the above transformation b. (3 pts) of the two regioisomeric reaction products shown, only one is observed to form under the...
Starting with the alkane (butane), please work the mechanism to get the final, aldehyde product. Please DRAW OUT the detailed mechanism and show ALL ELECTRONS on the reagents and the reactants along with the arrows pointing to the exact atom the electron(s) are being transferred to. Thank you SO MUCH in advance. I just really want to understand the mechanisms how the reagents rearrange the molecules via electron pushing. 0 OH butyraldehyde 1-butanol DMP NaOH Br Br 1-bromobut-2-ene 1-bromobutane H2/Pd,...
Please show mechanism and sterochemisty, thank you. Draw the product for the reaction below? н Br CH3 kto DMSO Draw the product for the reaction below? CH₃ Kt N- CHH DMSO
Quickly show all steps and answers all parts of the question please thank you 3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HCCH; OH H2SO4(aq) heat н,с (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(i).