can someone help me draw out the mechanism for p-anisidine and 1-bromo-2,4-dinitrobenzene with ethanol?
can someone help me draw out the mechanism for p-anisidine and 1-bromo-2,4-dinitrobenzene with ethanol?
The stereoisomer is meso but can someone help me draw and justify the mechanism Lab 13- Preparation of dibromosuccinicacid (due week 11) 1) Which stereoisomer of dibromosuccinic acid (racemic melting point 170°C, meso melting point 2900C) did you obtain? Draw it and show a mechanism to justify its formation.
how do I draw mechanism for the reaction of 2-bromo-2-methylpropane with AgNO3 in ethanol? also mechanism for the reaction of 1-bromobutane with NaI in acetone. please use arrows
Doing on a essay about ethanol for chemistry class. Can someone help me with an introduction pargraph about ethanol?
Could someone help me draw out the mechanism for this reaction? This was the description of the steps... Step 1) Ring opening of aziridine + MeOH addition Step 2) Acetylative debenzylation with Pd(OH)2 and acetic anhydride Step 3) Treatment with benzylamine in presence of Me3Al Scheme 3. Synthesis of (R)-1 from Aziridine-(2R)-carboxylate 10 PAN1 Meo HÑ BF3E12 OEt MeCN MeOH 90 °C, 3 h 93% OEt PdfOAC)2/C Meo Ac20, ETOH rt, 12 h OET DIN MOY NHBn HÑO Me:AI HNO...
Can someone show me the arrow pushing mechanism for this. Question 1. Draw the products of the following rea 1) Mg Br2) 。 OH
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
Can someone help me out with b and d? Thank you! Draw the major product expected in each of these reactions.
Could someone help me out on this problem. 1. Write the complete reaction mechanism for the following reaction. Show all electron flow with arrows and show all intermediate structures. NH2 H + 0.5-OO + H2O
Benzaldehyde and p-anisidine are dissolved in dichloromethane and can react to form (E)-N-(4-methoxyphenyl)-1-phenylmethanimine. Without using an acid catalyst or under any acidic reaction conditions, draw a step-by-step mechanism to show this reaction. Magnesium sulfate was also used in the reaction.
Would someone help me to solve these questions? Thanks in advanced Questions 1. Draw the mechanism of the formation of the diazonium salt from sulfanilic acid. 2. Draw the mechanism of the reaction of N,N-dimethylaniline and the diazonium salt of sulfanilic acid to form the azo dye. 3. Why does the dimethylaniline couple with the diazonium salt at the para position of the ring? 4. What would be the result if copper (I) chloride were added to the diazonium salt...