IVA. Predict the organic products formed in each of the following reactions of acetophenone. (12 points)...
Predict the major organic products formed in the following reactions. Be certain to indicate stereochemistry in products if it is important. H2O H2SO4 Br2 3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H:07, in your mechanism to indicate "acidic water"). (6 pts)
Predict the major organic products formed in the following reactions. Be certain to indicate stereochemistry in your products if it is important. H2 Pd/C HCI H2O H2SO4 Br2 Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H307, in your mechanism to indicate “acidic water”).
1. Predict the major organic products of the following reactions. Draw all stereoisomers that are formed. НО, OH 1 eq ,H2SO4 (assume H2O workup of reaction to neutralize product) 1. LDA 2. (assume H,O workup of reaction to neutralize product) 3. Hg(OAC)2 4. NaBH, EtOH 1eq HBr EtOH ambiente 1. Brz. CCL 2. NaOET, ETOH OH
Predict the products formed in the following reactions. Predict the product(s) formed in the following reactions. If there is no reaction, write “No Rxn" as the answer for the major product and leave the minor product box blank. If there is no minor product in the reaction, then leave the minor product box blank. If there are multiple products, make sure the products are in the appropriate box. (24 points, 4 points each) Note: Do not over complicate some questions...
Predict the major organic product or products of each of the following reactions: Identify the mechanism taking place in each of the reactions and please provide explanation. H2SO4 a) (CHỊ) CH CH=CH, HO Hg(OAc)2 NaBH4 b) (CH3)2CH CH=CH2 H2O BH3: THE H2O2, NaOH c) (CH3),CH CH=CH2 H2SO4, H2O d) CHCECH HgSO4 HZ/Ni f) + Cl2 + H2O g) Cold KMnO4 dilute h) 1. CH CO-OH 2. Hz0 Br2 i) CC14
help! chemistry predict the products and mechanism! the Product. Provide the stable organic product(s) for the reactions below. predict the Pro 1. Mgº, CH,CH,OCH,CH 2. CO (9) 3. H,O, HCI MgBr (X) 2. H,0,HCI 1. K Cr2O, H,SO, H,0 2. CH, MgBr (1 eq.) 3. H2O, HCI 1. Mgº, CH,CH,OCHCH 2. H20, HCI echanism. The following Grignard reaction has been observed to yield products A and B. MgCI THF-70 C 2. HCI, H20 0. Org. Chem. 1980, 45, 4952-4954. https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b01430)...
Draw the structurss for the product of pentanal and acetophenone with each if the following reagants. 2. Draw the structures for the product of pentanal and acetophenone with each following reagents: ΝΗΝΗ, LiAlH4 followed by H2O HOCH CH2OH, HCI ON NO2 , HCI H/Pt NH2-OH N2H4, KOH, heat H2CrO4, heat Ν-Η .HCI PhP-CH-CH-CH(CH3)2 + Buki Zn(Hg)/HCI NaBH, in CH3OH/H20 Na2Cr2O7 PhNH2 PhNHNH2 HANN -NH2 Organic Chemistry II Dr. Mirjafari
Predict the organic products of the following Grignard reaction. Ma 1) CH3MgCl (excess) Et20 2) H30 Complete the mechanism for the above reaction below. Add any missing curved arrows, bonds, atoms nonbonding electron pairs, and charges
Predict the product or provide the mechanism Predict the Product. Provide the stable organic product(s) for the reactions below. 1. Mgº, CH3CH,OCH CH3 2. CO2 (g) 3. H2O, HCI W MgBr (xs) 2. H2O, HCI 1. K Cr2O7, H2SO4, H2O 2. CH3MgBr (1 eq.) OH 3. H2O, HCI 1. Mgº, CH3CH2OCH2CH3 2. H2O, HCI Mechanism. The following Grignard reaction has been observed to yield products A and B. 1. Me Me MCI THF, -70 °C SOH OH ole er periodo...
E to H please I. Predict the major organic product formed in the following reactions a) o KOBut HOBut b) KOBut HOBut öt CH CH; CH_CH CH KCN Acetone н d) solvent alkyl halide nucleophile CH e) H -Br KOBut HOBu' Br- -H CH f) Br CH,CH OH two products formed ♡ + CHI h) Br NaOCH3