please show the mechanism and reasoning, thank you so much in advance!
please show the mechanism and reasoning, thank you so much in advance! DER . . M...
Please show the mechanism of the following reactions. Thank you so much in advance! Не осн, H5C, осна H5C Br + HBr CH3OH 25 °C 50% 50% H,0 . + Br° . . ~ + снҳон 60 °C + ~ ~ о но Br Acetone 50 °C . . .ю° сьон Д. но во 60 °C . в . сноснон , нве HBr 75 °C
Please solve, Draw the major product(s) and show the mechanism. Thank you so much, i really appreciate it. CH3 H3C CH3
please explain in detail. Thank you in advance . 1. Circle the mechanism (SN2, SN1, E2, or E1) responsible for the formation of each product in this reaction. If the product cannot be formed in the reaction, circle "not a product". (2 pts) CI CHE CH3 CHE CH3 осна SN2 SN1 E2 E1 S2 SN1 E2 E1 SN2 Sn1 E2 E1 SN2 SN1 E2 E1 not a product not a product not a product not a product 2. These reactions...
also please explain why. thank you in advance These reactions do not afford the major product that is shown. Draw the structure of the major organic 2. product that is actually formed. (2 pts) Hасо H3CO NaOH Br STETET (CH),cок" (potassium t-butoxide)
Please show work as neatly as possible, thank you so much in advance! The auxiliary equation for the given differential equation has complex roots. Find a general solution. y" - 6y' +45y = 0 y(t) =]
Please be detailed as much as possible. THANK YOU VERY MUCH! Show the synthesis mechanism of the reaction sequence shown below . . + Na NM, 2-CH(CH, CHO ; 3. H* (quehchi n); 4. 4/Pa (fe, IParid ioe 55. ) / 40, hydrogenation of 3-hexyne 2. Show the intermediates and the products in the trans (CH₃ CH₂ C = CCH₂ CH₃) with Na/NH3 (liquid)? o. What products will form upon ozonolysis 10 lexcess) and reductive work up can lH20) of...
all 3 questions please. thank you in advance!! Question 8: Draw the Syl and El products formed in the reaction of (CH3)3CBr with H,0. Show mechanism using arrows." CH3 CH3-C-Br + CH H-O-H Question 9: Draw the major E2 elimination product formed from the following: alkyl halide. Question 10: Give structures corresponding to each name. a)-7,7-dimethyl-4-octanol b)>5-methyl-4-propyl-3-heptanol" c)-2-tert-butyl-3-methylcyclohexanolº d)- trans-1,2-cyclohexanediol"
Please show work as neatly as possible, thank you so much in advance! Decide whether or not the method of undetermined coefficients can be applied to find a particular solution of the given equation. 60''(x) - 70(x) = 4x sin 2x + 4x cos 2x Choose the correct answer below. O O Yes No
Thank you so much! (2 pts) Draw the major elimination products and Identify the mechanism responsible (E1 or E2). If both E and Z isomers form, only draw the E alkene. If only one isomer forms, label the alkene "E,""Z," or neither 1. NaOCH3 а. Br НОСHЗ b. НОСНЗ C. CI NaOCH3 d. (6 pts) Draw the substitution and/or elimination product(s) for the following reactions and identify 2. the mechanism responsible (SN1, SN2, E1, or E2) for each product drawn....
help please im so lost...as much detail with explainations for the mechanisms 1. For the reactions below: (l) draw all elimination products that would form under the stated conditions, (2) circle the major products). (3) determine how (El or E2) and (4) explain your reasoning (45 p) CH OH 2. Provide a mechanism which explains the following conversion (pt) xriy For the reactions below: (1) draw all products that could form under the stated conditions, (2) determine how they formed...