Complete the reaction giving the reactants for this product KOH/EtOH
Please explain clearly and give the direct answer
Complete each reaction by giving the major product: Nal in EtOH solvent 11lll Melman Nal in acetone solvent EtOH in H2SO4 t-butyl alcohol (a) All Snl reactions occur with inversion of configuration. True or False (b) The rate-limiting step in a Syl reaction always yields a carbanion. True or False
Closing Activity ons below by either giving the product or the reactants ofthe following reaction. If a particular reaction is not possible, put "no reaction". он 0 Nao 0 HN N(Et)a soci 0 0 0 он Bonus: Compare and contrast nucleophilic carbonyl substitution with nucleophilic carbonyl addition Addition Both Substitution
for the reaction: acetaminophen + (NaOH/EtOH note: etoh is ethanol) and butyl iodide ---------------> 4-butoxyacetanilide a) The first step in this reaction is to reflux acetaminophen in a NaOH/EtOH solution, followed by the addition of butyl iodide. What is the purpose of using the NaOH/EtOH solution? Would the SN2 reaction still occur if the first step was not completed? Why or why not? b) Upon completion of the reaction (before filtration), an additional 4.0 mL of 1.0 M NaOH/EtOH was...
It is hard to read but it says AgNO3/EtOH
3. Give the complete reaction mechanisms, showing reactants, intermediates and products for the reactions of 1-chloro-2-butene in AgNOEtOH. You do not need to show transition states. Show appropriate stereochemistry 3b. Would you expect the product(s) to be optically active? Explain.
complete the following reaction equations. explain product
formation and conditions.
rond NaOET EtOH 91 % 9%
complete the following reaction equations. explain product
formation and conditions.
он 1. N(CH3)3 EtOH CH3OH
Complete the following reaction sequence. giving details of all Complete the following reaction sequence. giving details of all significant
Complete the following reaction scheme, giving complete
stereochemic details as relevant. Explain please!
Complete the following reaction scheme, giving complete stereochemical details as relevant. Note: Be alert to the possibility of rearrangements OH t-BuOK, t-BuOH. heat heat i. KMnO4. ОН. 2 120,heat? (major product) ? (major product) + ii. H,0 HBr NaBH4 i.BHy,THF ii. H202. OH ? (major product)
5. Complete the following reactions by filling in the missing Reactants, Reagents, or MAJOR Product. If TWO products are equally formed show BOTH. 1. DIBAL 2. H307 Colon - ohne кон ОН OH NH2 LIAIH4 1. LDA / Dry THE - to 1.LA/D THE 1.1.2 Equiv. LDA/THF 2. Br Br2 acetic acid Pyridine Heat Nat Et EtOH single product
What will be the MAJOR product of this reaction? EtoNa EtOH Br a) b) c) What is the MINOR product of this reaction? EtoNa Br EtOH 11 a) b) c) What will be the MAJOR product of this reaction? OH H2SO4 heat a) b) c) d) What will be the MAJOR product of this reaction? H2SO4 heat HO) a) b) C) d) 며 OA What is the LEAST stable carbocation pictured? a) CH. b) d) What will be the MINOR...