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- Click the "draw structure" button to launch the drawing utility. Draw the product formed wvhen the following compound is treated with two equivalents of CH3CH,CH,CH,MgBr followed by H,O. of OCH, draw structure ...When norbornene undergoes hydroboration-oxidation, a mixture of two stereoisomers is produced in a roughly 6:1 ratio. (a) Draw both of these isomeric products. (b) Which product is favored? Hint: You should build a model of norbornene and consider the transition state leading to each product. 1. BH3 THF ? 2. H2O2, NaOH, H,O NorborneneI'm really confused on how these products are formed, could someone please explain or draw arrows to help me under i will really appreciate it !
- Draw the principal organic product for the reaction of 2-bromobutane with magnesium in diethyl ether, followed with benzaldehyde in diethyl ether, and then followed by dilute acid...Click the "draw structure" button to launch the drawing utility. What alkene is the major product formed from the following alkyl halide in an E1 reaction? CI The major product is: draw structure ...Tautomerization is a process in which an enol yields a ketone Give one examplefor a keto to enol tautomerization. Which form is more stable. Also, which ismore stable the E isomer or the Z isomer of 2-Chloro, 2-Butene
- Synthesize Chloramphenicol from Toluene or Benzaldehyde. Draw and explain step by step please.(p.s: if you can, can you write what the reagents does?) (Drug Chemistry)15) There are two parts to this question (a & b), be sure to answer both. (a) frs) When (R)-alkyl halide shown is allowed to react with CH3S-Nat, an optically active product is formed in high yield. Draw this product(be sure to show/write stereochemistry). KELEN H₂CH₂C Br (b) you arew. (R) H H₂C Optically active alkyl halide +CH,SNa Acetone 340-SONG Optically active product 3) For the reaction in part (a), show a mechanism for the formation of the products thatQ4: Explain: Friedel-Crafts acylation formed by attack at the meta positions of Nitrobenzene. (-NH; and -OH) act as powerful activators toward electrophilic aromatic substitution.
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