


Provide mechanisms for the reactions shown H30* Enamine formation H30* OHNNH2 1. LiAID + En 2....
Free Response Section Provide the products formed when the cyclic dostal shown is hydrolyzed with acid. You must provide a curved arrow mechanism to show how the asetal breaks down into the products. ( pes) H,0* heat 11. Provide the mechanisms for the reactions shown. (30 pts) CH,COH Baeyer-Villiger Oxidation Enamine formation
Provide the products and mechanisms of the reactions of 1-methylcyclohexene with the following reagents: A.) CHBr3, OH- B.) Simmons-Smith Reagent C.) H+, H2O D.) 1. BH3 * THF, then 2. OH-, H2O2 E.) 1. Hg (OAc)2, H2O; then 2. NaBH4 F.) H2, Ni G.) Br2 H.) Br2, H2O
3. MECHANISMS: Provide complete, arrow-pushing mechanisms for each of the reactions shown below. Only TWO of these will be graded but YOU MUST COMPLETE ALL FOUR TO EARN ANY CREDIT! (8 pts.) (note: only mechanism for step 1) 1. Hg(OAc), CH3OH H20 H2SO4 tocha 2. NaBH
Please help with both if possible!
1. Provide the missing reactants or products for the reactions shown below. Provide the structure(s) in the boxes provided. (8 points) a. Na o= 1. CH3Mgi 2. H30 2. H:0* 1. CH3Li 2. H30* 2. Provide the reaction mechanism for the reaction shown below. (4 points) cat. H ОН + H2O ОН
5 2. Predict the products of the following reactions. HOOH H30+ 1. excess CH3CH2MgBr 2. H30* H30* 8 carbonyl and amine H30* 3. The following reactions are incorrect, showing the wrong product (or at least not the major product). Please provide the correct product and a brief explanation. HO 2. excess CH3LI 3. H30* Correct Product H30* Correct Product
(27 points) Draw “arrow pushing” mechanisms for THREE of the
reactions in question 1
1) (27 points) Provide the missing reactants, reagents or products 1) NaBH4 2) H30+ H30+ H =- Nat COH H2N. NH2NH2, KOH & www.ro 1) onto ✓ I H 2) H30+ Croz H2SO4 HO H20 1) Mg, EtOEt 2) D. wa PH 3) H30+
In the reactions below you are given a product and enough the starting materials information about the formation of the product to provide 1. Th followling as munde usiig a Dicls-Alder reuction Provide the rouctants and reaction conditiows The foliowing product was made starting with benzene -provide all steps of the reaction and reaction conditions 2. 3. The following was made in an enamine synthesis-provide the starting materials and reaction condit Aromaticity-3 points each Please classify the following compounds us...
6. Provide the mechanisms for the following reactons MgBr 1. Excess OH OCH 2. H30 som HB HBr 1. LIAIH4 O2. H30+ 7. Suggest a structure for an unknown A whose formula is CH160 and gives the following chemical test results. Formula C6H100 Hydrogenation Test H/Pt Chromic Acid Test HaCrO4 Lucas Test HCI/ZnCl2 • Reacts to give C H20 Reacts, turns green/brown, precipitate for Reacts, a new oil layer forms on top.
1. Provide the products for the following reactions (2 points, 1 point per question). 1) NaOH, Br2 2) H30+ pentanol, H2O+ 2. Draw the mechanism for the following (1.5 point). ethanol, H30+ ОН 3. If you were doing the reaction shown in #2 in lab, how would you use IR to determine if you formed the product or a mixture of product and starting material (0.5 points)? 4. Draw the 'H-NMR for the structure below. Label each peak on the...
Name: Aexab yard Chapter 10: Mechanisms 1. Provide a mechanistic explanation for the formation of the observed products in the following cat. H50 heat 2. Draw an arrow-pushing mechanism to justify the following transformation. OH heat Write a plausible arrow-pushing mechanism for the reaction depicted. Make sure that you account for the stereochemistry shown. 3. Br Br2 MeOH OMe