provide products 2. Provide the structure of all intermediates and all products 1-14. 1. NOCH 2.11,0...
Calibri Light 20 B IC A 2. Provide the structure of all intermediates and all products 1-14. 1. NOCH 2.H.O. COM acid catalyst hint: - BUOH 2 Nai 3, H49 heat 1.(CH,,Culi.cther 2. H,09 1. NOCH 1.HO uinti Page 1 of 4 A po PC,CH NaHCN 1.31 quv NDH 1 LA 2.HO 2. H.O 3 Hàn ( N 1. LIATH ZHO LCH Mc
Help with the following question! thank you! Provide the structure of all intermediates and all products -NH2 PCC, CH.CL2 NaBH CN OH 7 1. 3 equiv. 12 4 equiv. NaOH 1. LIAH 2. HO 2. H,0 10 2 equiv. (CH3)2NH 1. LiAlH 2. H20 11 12 1. CH MgCl 2. H,0 H,00 13 14
iupac name 1. Give an acceptable IUPAC name for these two compounds. 2. Provide the structure of all intermediates and all products 1-14.
3. Provide the intermediates/products for the following reactions. 3. Provide the intermediates/products for the following reactions 1. BH3. THF 2. H20s NaOH, H2O CH3 1·LDA,-78°C, THF 4. H2O 1. Na CroO HSO, HO 2. SOCl2 Bn
1. (2 pts) Provide a mechanism and missing intermediates for the following reaction. Account for all the intermediates and final products, OS IÓ Н,0
1. (2 points) Provide the IUPAC name for the following structure. он 2. (2 points) Draw the structure from the provided name: 5-chloro-2,2-dimethylcyclohexane-1,3-dione. 3. (6 points) The following reaction produces five different substitution and elimination products, (a) Draw these products and (b) rank the stability of the elimination products by using the labels (E1-E3) according to the products as you have entered them. substitution product S1 substitution product S2 HzC04 CF, H-OH elimination product E1 elimination product E2 elimination product...
8. Provide all the products for each reaction below (no arrow pushing or intermediates). You do not need to label major or minor products or the type of reaction. Et-OM DBN DMSO Foxit HC- DMF Inercih DISC
Provide structures for the reactants, intermediates, or products, as indicated, in the following reactions. Draw the structures in the boxes provided. NBS Br ether NBS, CCL 2. KOH, ethandl
5:43 PM Thu Oct 31 29% Chem2542 Assignment-6.doc 1. Provide the structure of diene and dienophile required for the synthesis of the following compound via Diels-Alder reaction. Ph сно сно 2. The following a,b-unsaturated ketone can react with nucleophilic reagents to yield 1,2-addition as well as 1,4-addition (conjugate addition) products depending on the nucleophilic reagent. Provide the structure of the major primary 1,2-addition or 1,4 addition product formed in each reaction 1. CH,MgCI 2. HC 1. LIAIH 2. HC 1....
Provide a full mechanism for the synthesis of 3-acetyl-7-(diethylamino)-2H-1-benzopyran-2-one. Include all formal charges, resonance structures, intermediates and products. Use proper arrows for electron flow, vaguely drawn arrows will not receive marks.