6. For the following reactions tell whether they will react under condition on condition (Nal/acetone) or...
6&7 please 6. For the following reactions tell whether they will react under Secondition condition (Nal/acetone) or neither. Also indicate the product formed if any (10 points Mechanism Product (S.1 or 2) my НАС " H₂C CHO 7. Draw the major product expected in each reaction below. (10 pts) HAPO. HC CH3 heat OH CH3CH ONa нсін CH,CH OH 55°C B CH2CH3 KSH (1 mol equivalent) acetonitrile он acetonitrile
6. For the following reactions tell whether they will react under sa condo non, hea), condition (Nal/acetone) or neither. Also indicate the product formed i (10 poi Mechanism Product (S.1 or 5.2) 7. Draw the major product expected in each reaction below. (10 pts) CH₂ H₃PO, H₂ CH₃ heat OH Hoogte CH,CH, ON CH,CH, OH 55°C il. B YCH CH3 HCO KSH (1 mol equivalent) acetonitrile OOH acetonitrile Dr. Denton
6. For the following reactions tell whether they will react under Ss1 condition (EtOH, heat), Ss2 condition (Nal/acetone) or neither. Also indicate the product formed if any. (10 points) Mechanism Product (Sl or S2) Br TsO HaC ii. Br Br HC iv. H3C CH3 H3C OCH3
1. Use numbers to indicate which compound will react the fastest by the S2 mechanism these alcohols with Nal in acetone With 1 beine the fastest and being the slowest CH HH HO 2. Show the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) OH con HB CHE HCX H₂C CHS Sul condition HyC CH CH Loh 1 Ca H₂C nhạc ,
1. Use numbers to indicate which compound will read the fastest by the these alcohols with Nal in acetone. With 1 being the fastest and being the sot 2 mechanismo Hgc er HOCH HC 2. Show the step by step mechanism to account for the following transformation. Also predict une major product formed. (20 points) com, HB HCX HBOX Br HACCHE Syl condition CH нус сн, он orts CH H₂C Dr. Denton
Quickly show all steps and answers all parts of the question please thank you 6. For the following reactions tell whether they will react under Syl condition (EtOH, heat), SN2 condition (Nal/acetone) or neither. Also indicate the product formed if any. (10 points) Mechanism Product (SN1 or SN2) 11. Tso H₃Ct iv. НАС HC CHE
could someone answer these for me please 1. Use numbers to indicate which compound will react the fastest by the Ss2 med these alcohols with Nal in acetone. With 1 being the fastest and 4 being the slowest (10 ne lastest by the S2 mechanism for нс , H₂C нсон, Br H₂C * now the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) CHE conc. HBr CH, HCM Syl condition...
1. Determine whether the following reactions will go through SN1, SN2, E1, or E2 mechanism a. 1-bromobutane + sodium hydroxide b. 2-chloro-2-methylpentane + sodium hydroxide + heat C. 2,3-dimethyl-3-bromopentane + water d. 2-bromobutane + methanol 2. Draw the major product for the following reactions (draw both products if racemic): NaSH DMSO TsO CHA Nal CH, acetone CH,CH,ONa+ ethanol CH,OH/H-0 Solite Nal (1 equiv.) acetone F CH2CH OH 25°C
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium (D) or not. (20 pts) HC CH, ОН TH 0 H,SO.(aq) heat D HC NaOCH.CH CH2CH,OH heat CH, (ii) Write a detail mechanism for the formation of the product in question 30). 4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts) НО. Dr. Denton
answer all please 17) What is the major product in the following reaction ? (CH3),C.O-OH, OsO. (cat) t-butyl alcohol, OH Page OH HO но он OH OH On 18) Which one of the following reaction steps work best to carry out the transformation shown below? A) 1) CHI C) 1) CH,COOH B) K,CO, in Acetone, Butyl bromide D) 1) H2SO42) CH,COOH 19) Write the product of the following reaction 1) NaCN, water 2) H2SO4 ONa ON CNC 20) Write the...