please help 2. 3 pts) Lithium disopropyl amide (LDA) could theoretically act as a nucleophile or...
(3 pts) Lithium diisopropyl amide (LDA) could theoretically act as a nucleophile or a base. With that in mind, draw the four theoretical products (3 from E2 and 1 from SN2) of the reaction below. Then, circle the major product. Provide a brief rationale. 2. Br N Li
Please help :(
Chad Landrie tudent Name:, Class Day/Time: (4 pts) Draw the major product for each series of reactions o bonup d mainsdo swb.bo ao012 1 alo b onos es motb o a o orl ue s o noa a. BoHe, diglyme b. NaOH, H-O2 c. MsCI, py d. NaCN, DMSO a. HBr, peroxides b. KOC(CHa)3, DMSO с. Вгр СH-Cle a. HBr, CH2Cl2 b. KOČ(CHa)a c. HBr, peroxides d. NaCEC-CH3 H2, Pd/CaCO3 CHa CH,CH,он Pb(OAc) Phi (3 pts) Lithium...
CHEM 3020 Practice exam 3 Give the major organic product for the following reactions: R0, H.2 HO HO Bry 1) Lithium Disopropylamide (LDA) 2) CIES o spomen 1) Lithium Disopropyl anide (LDA) OCH, CITOTT 1) OHI 2) CHI OH Give all possible products from the following mixed aldol reaction and show how they can be formed. Show the mechanism for the keto enol tautomerization of 2-propanone in both acid and in base.
could someone please help me out in organic chemistry?
Last Name- - First Same 1. Write the products of the following reactions. If there is no reaction write NR (30 points). a) CHCH.CH-Br + 2Li => "X" +LiBr: X=? C) 2 "X" + Cul Lil + "Y": Y- S and water d) (U) Y + 2. Starting from CH CH Br and diisopropyl amine, describe how you would prepare lithium diisopropy! amide (LDA), LINR, where R=Isopropyl (5 points) 2. Starting...
CHEM 3020 Practice exam 3 Give the major organic product for the following reactions: R0, H.2 HO HO Bry 1) Lithium Disopropylamide (LDA) 2) CIES o spomen 1) Lithium Disopropyl anide (LDA) OCH, CITOTT 1) OHI 2) CHI OH Give all possible products from the following mixed aldol reaction and show how they can be formed. Show the mechanism for the keto enol tautomerization of 2-propanone in both acid and in base.
1. Under second-order conditions (strong base/nucleophile),
SN2 and E2 reactions may occur simultaneously and
compete with each other.
Show what products might be expected from the reaction of
2-bromo-3-methylbutane (a moderately hindered 2∘ alkyl halide) with
sodium ethoxide.
2.Under second-order conditions (strong base/nucleophile),
SN2 and E2 reactions may occur simultaneously and
compete with each other.
Show what products might be expected from the reaction of
2-bromo-3-methylbutane (a moderately hindered 2∘ alkyl halide) with
sodium ethoxide
3.. Provide the structure of...
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....
please help
For the reaction below provide all possible product(s), hand draw the products on a piece of paper and circle the major product. No cutting and pasting from the Internet, You can only upload an image of your response, Initial your name next to each response. Br PhzP Butyl Lithium 2 Butanone ether ether Br
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...
poease answer and explain all. thank you!
3. Acids and Bases. (15 pts) (a) Circle the weakest acid in each series shown below (9 pts). Series 1 HC CH2 Series 2 OH он OH Series 3 Cl ai pk, 9.38 pk, 10.2 (b) Draw the products of the following acid-base reaction (6 pts). CH3O reactants products 4. Use curved arrow to indieate the flow of electrons for the following elementary steps. Label each step with a proper name such as...