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- Organic Chemisrty study guide help. I need help with this question and have no idea how to do it. It says, "Draw all possible chlorination products of the following reactions:"Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. Do not neglect stereochemistry. NaCN DIBAL Br в A "OCH3 (sodium cyanide)These are all electron-withdrawing groups that slow electrophilic aromatic substitution, with one exception. Which one? © CO,H O NO₂ O CF3 O NH2
- Which synthetic route is the best way to prepare ethyl isopropyl ether? O (CH3)2CHONA + CH3CH2Br O CH3CH2ONA + (CH3)2CHBr O CH3CH2ONA + (CH3)2CHOH O CH3CH2OH + (CH3)2CHOH + H2SO4, 140 OCAlkyl diazonium salts are unstable even at low temperature. They decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes) rearrangement. Keeping this in mind, draw a stepwise mechanism that forms all of the following products. NANO2 он + HCI, H2O NH2 онComplete the following addition reaction by providing the missing product after protantation. Indicate regiochemistry and stereochemistry when relevant. NaOH OA. но он Но он OC. но OH B.
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