complete the missing reagents 앤 요 OCH b) 운 꼭 d) f) ОН """ -Br CO2H...
Q2) Complete the missing reagents
Q3) propose one way to synthesize the products using Grignard
reagent
PLS HELP!! thank you
Q3) Propose one way to synthesize the products using Grignard reagent. a) d) g) ОН ОН ОН b) e) h) ОН ОН ОН ОН f) ОН Q2) complete the missing reagents a) ОН ОН olan OCH3 b) ОН -Br d) ОН -Br CO2H е) 9) -СІ ОН ОН
Identify the reagents used in the following synthesis 1. Cl Br он он b. он он d. OCH3 C. e.
Identify the reagents used in the following synthesis 1. Cl Br он он b. он он d. OCH3 C. e.
3. (20 points) Complete the following by adding the missing reagents) or major organic prodacet) он 1. CH CH,MgBr 1. Na 2. PhCH Br CH,CHO NaB 14. When a ketone is treated with LiAIH, followed by addition of H,O, what general class of product results? e) aldehyde b) secondary alcohol c)tertiary alcohol d) ether a) primary alcohol 15. What are the expected products of the reaction of PhOCH, with 1 equivalent of concentrated HI? b) phenol and methanol a) phenol...
Q7.1 6 Points Br OH OH CI Br F А D E OH ОН. H2N- F G H J Which of these rings is OPTICALLY ACTIVE? (select all that apply) Compound A Compound B Compound C Compound D Compound E Compound F Compound G Compound H Compound Compound J None of these Q7.2 3 Points Br OH OH CI Br F А B с D E OH OH xazk HN F G H Which of these rings is MESO? (select...
4... Which structure or structures represent the enantiomer of the following molecule? он OCH он он он он H3COli OCH Осн; mOCH Br Br Brl I IV II III a l d. IV e I and V b II C.ID
propose suitable reagents
1. Br ОСН3 і — b. он Br c.ro он Оң 8. — - 4) Х он г.
kill 7.33 Identify the reagents you would use to accomplish each of the followiing transformations: Br OH (a) OH (b) SH Br (c) OH (d) Он Br henodut (e) Br xo ne to bse _ (f) Br ОН (g) (h) 160
6 d.) ethylene OCH Bra, FeCl3 f.) OCH, Clz, FeCl3 g.) CH30. cyclopentene CH30 h.) ОН 1. NaNO2, HCl(aq) 2. Kl(aq) NH2
CO2H CO2H HNO3/H2SO4 H20 2. +conc. HBr H20 Br OH a Electrophilic addition b E2 Elimination c-SNI Nucleophilic substitution d S2 Nucleophilic substitution e-Electrophilic aromatic substitution f-carbonyl nucleophilic addn g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn for your answers 1. 2.
For each of the following questions, provide the missing reagents (that can be purchased) and conditions or predict the MAJOR product. Indicate stereochemistry and identify a racemic mixture if applicable. If no reaction occurs, write out "no reaction." . a. d. Ag,O/NH,OH "ОН e. 1) CH (CH,),Br/ 2 Li 2) HCI f но но но. (:) g. н NH NH