Question & Answer: A) NBS B) Br_2, CCl_4 C) Cl_2, CCl_4 D) HBr E) HBr, ROOR F) H_2O G) Hg(OAc)_2,…..

Cl CI OH A) NBS B) Br2, CCl C) Cl2, CCl,4 D) HBr E) HBr, ROOR F) H20 G) Hg(OAO2, NaOH, H2O H) HgSO4, H2O, H2SO4 1) H3O* J) (sia)2BH K) BH3 L) H202, NaOH, H20 M) Pd N) Lindlars Catalyst O) 1 % Pd(OAc)2, R3P P) NaBH4, CH3CH2OH R) (CH33COK, (CH3)3COH S) NaNH2, NH3 T) Na, NH3 U) H2 V) 03 AE) 8 (rkup) 2304 W) Zn, CH3coo X) CrO3, H2SO4, H20 Y) CH3CH2Br Z) CH3CHCH2Br AA) CH3CH2Li AB) CH3C2CH2Li AG) - 0 Al) Look at the given synthesis and the provided reagents. Fill in the blanks with the single letter code of the appropriate reagent, or the appropriate descriptive vocabulary word/phrase to complete the description. Remember the computer is very literal so check your spelling carefully. First we add reagent followed by equivalents of reagent followed by workup to give the functional group Then we add reagent followed immediately by reagent and work up to add the needed carbons. Then reagents and will give the (functional group) with stereoselectivity. Lastly reagent will give the final product with stereoselectivity

A) NBS B) Br_2, CCl_4 C) Cl_2, CCl_4 D) HBr E) HBr, ROOR F) H_2O G) Hg(OAc)_2, NaOH, H_2O H) HgSO_4, H_2O, H_2SO_4 I) H_3O^+ (workup) J) (sia)_2 BH K) BH_3 L) H_2O_2, NaOH, H_2O M) Pd N) Lindlar’s Catalyst O) 1 % Pd(OAc)_2, R_3 P P) NaBH_4, CH_3CH_2OH Q) CH_3CH_2ONa, CH_3CH_2OH R) (CH_3)_3COK, (CH_3)_3COH S) NaNH_2, NH_3 T) Na, NH_3 U) H_2 V) O_3 W) Zn, CH_3COOH X) CrO_3, H_2SO_4, H_2O Y) CH_3CH_2Br Z) CH_3CH_2CH_2Br AA) CH_3CH_2Li AB) CH_3CH_2CH_2Li Look at the given synthesis and the provided reagents. Fill in the blanks with the single letter code of the appropriate reagent, or the appropriate descriptive vocabulary word/phrase to complete the description. Remember the computer is very literal so check your spelling carefully. First we add reagent followed by equivalents of reagent followed by workup to give the functional group Then we add reagent followed immediately by reagent and work up to add the needed carbons. Then reagents and will give the (functional group) with stereoselectivity. Lastly reagent will give the final product with stereoselectivity.

Don't use plagiarized sources. Get Your Custom Essay on
Question & Answer: A) NBS B) Br_2, CCl_4 C) Cl_2, CCl_4 D) HBr E) HBr, ROOR F) H_2O G) Hg(OAc)_2,…..
GET AN ESSAY WRITTEN FOR YOU FROM AS LOW AS $13/PAGE
Order Essay

Expert Answer

Organic chemistry

First we add reagent B followed by 2 equivalents on reagent S followed by F workup to give the functional group alkyne. then we add reagent S followed immediately by reagent AI and I workup to add the needed carbons. These reagents T and C will give (functional group) alcohol with anti stereoselectivity.

Still stressed from student homework?
Get quality assistance from academic writers!