Can someone help me with this by showing the stepwise mechanism of how we form this...
Please help provide stepwise mechanisms for each product with arrows 1. (5.75pts) Provide a stepwise mechanism showing how each of the products below are formed OH H,SO
4. Write a complete stepwise mechanism showing how each product will form. heat CH,ОH ОСНЗ OCH3 Br
Can someone help me draw the mechanism for this reaction? Please include all the arrow movements involved in the reaction and the CHIRAL CENTERS present. Any enantiomers, if any. Thanks. OTBS OH TBAF, THF rt, 8-18 h 82-98% 5a-c 6a-c
Could someone help me by showing a detailed step-by step ARROW-PUSHING MECHANISM for the above reaction?Thank you! C1S02NCO Cloche a C1-S-N-CEO AN H20 10H NH A 0 0-30 OH با قمر
Can someone help me with these please? Thanks! A2. Predict the product in each of the following reactions. If no reaction write NR. e) O C LDA b) OH -OEt c) -OEt d) g) LDA LDA
Can someone help me do the derivation? How can we go from equation 7.58 to 7.59 in details? Please help<3
can someone please help me with this page??? thanks in advance!! 4. Predict the products for the following reaction sequences. Он sOc/2 1. LIAIH 2. Hо (CH3)2NH (a) pyridine CH3Br base (-HBr) CH3CH2Br base (-HBr) (b) NH2 Br NaN3 (a) LIAIH (c) (b) Н-О MCРВА NaN3 (a) LIAIH4 (d) oH(a) NH2 NaBH3CN (e) H2SO4 5. Predict the major product for the following reactions. 1. excess CH3 NH2 (a) 2. Ag O, H2O heat 1. excess CH (b) 2. Ag20, H2O...
please help me solve both of these!! Write the complete stepwise mechanism for the acid catalyzed hydrolysis of the compound shown. Show all intermediates, indicate with curved arrows the movement of electrons and show all formal charges and lone pairs of electrons where relevant. Write the structure of the Michael addition product and the final Robinson annulation product when using the following starting materials. Hint: the dialdehyde is the Michael donor and the ketone is the Michael acceptor. Н Michael...
Provide a stepwise mechanism for the multi-step synthesis of Benzocaine. The overall reaction can be seen above. Please show every step- thanks! NH HN-C-CH; 1) KMnO4, MgSO4 HN-C-CH; (CH3CO)20 CH; 2) H2SO4 HO СН3 p-acetotoluidide COOH p-toluidine 1) HCI, 2) pH 7 H2O, A NH2 CH3CH,OH H2SO4 HOⓇO CH3CH2O o Benzocaine PABA We wish to oxidize the methyl group of p-toluidine but cannot do so without oxidizing the amino group (NH2). Consequently, the first step of our lab synthesis of...
Can someone please help me figure out how to use a ti 84 calculator to do E, F, G, and H. Thanks in advance.