4. Draw the missing products for each transformation. Show stereochemistry when needed. a. CH3 S b. C. d. e. f. HI Br₂/H₂O CH3 1. BH₂, THF -CH3 2. H₂O2, NaOH, H₂O CH3 1. Hg(OAc)2, H₂O 2. NaBH H₂ CH3 Pd 1.03, CH2Cl2 2.Zn, HOẶC
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- 6. Identify the best reagent(s) for this reaction. (see attached screenshot). a. H2SO4, HgSO4, H2O b. 1. Disiamylborane, 2. HO–, H2O2 c. K2Cr2O7, H+ d. NaOCl e. H2, Pd1. Which of the following is the strongest nucleophile? Refer to the diagram below with an MeOH, MeSH, etc. 2. Which of the following is true about the stereochemistry of SN1 reaction?a.retention of configuration at the electrophilic centerb.50:50 mixture of retention and inversion of configuration at the electrophilic centerc.inversion of configuration at the electrophilic centerd. slightly more inversion than retention at the electrophilic centerMaking sure to pay attention to stereochemistry, what is the main product for each reaction?
- These reagents can produce ketones with alkynes A. BH3, THF, H2O2 B. KMnO4 C. O3 D. H2SO4, H2O, HgSO4 choices:A,DB,CA,B,CA,B,C,DWhich of the following reagent best accomplish this transformation below? a. BH3, THF, H2O2 b. NaNH2, NH3 c. H2SO4, H2O, HgSO4 d. H2, LindlarWhich compound will undergo solvolysis most rapidly? A. t-hexyl-I B. t-hexyl-OSO2CH3 C. t-hexyl-F D. t-hexyl-OSO2CF3
- Rank the nucleophiles in each group in order of increasing nucleophilicity. a.−OH, −NH2, H2O b.−OH, Br−, F− (polar aprotic solvent) c.H2O, −OH, CH3CO2−For problem 8.17, all of the reactions will be SN2. For each reaction, identify and evaluate each nucleophile (strong? weak? Strong or weak as a base?) Also, evaluate each solvent as polar protic or polar aprotic. I recommend drawing the structure of each solvent. (g) Sodium methanethiolate (NaSCH3) in ethanolCan you match best nucleophile / conditions from the list that will give a successful hydrolysis reaction for each electrophile? (there's one best nucleophile / conditions for each electrophile) <List for Nucleophile / condition> a. LiAlH4; hydronium work-up b. PCC c. NaH d. CrO3 e. HOEt f. H3O+ or OH- g. H2O h. NaBH4;hydronium work-up Electrophile 1. Acid chloride 2. Acetic anhydride 3. Ester 4. Amide I'm asking again on bartleby because pther tutor gave me the right answer because I think I didn't make my question clear enough.
- The missing reagent should include a bromine atom. and the final product should show stereochemistry.For problem 8.17, all of the reactions will be SN2. For each reaction, identify and evaluate each nucleophile (strong? weak? Strong or weak as a base?) Also, evaluate each solvent as polar protic or polar aprotic. I recommend drawing the structure of each solvent.Consider 3-iodo-2,3-dimethylpentane and 3-iodo-2methylpentane. a. which reacts faster in an Sn2 reaction? Explain. b. which reacts faster in an E2 reaction? Explain.