Which route from the choices listed below is the best procedure for the reaction shown below?...
which route from the choices listed below is the best procedure for converting 3-phenylbut-1-ene to 3-phenylbutan-1-ol Which route from the choices listed below is the best procedure for converting 3-Phenylbut-1-ene to 3-Phenylbutan-1-ol? -OH a. i. HCl; ii. NaOH b.i. Hg(OAc)2; ii. NaBH4 с. Н30* d. i. BH3; ii. H202, NaOH, H20 e. NaOH, A f. H202
Which route from the choices listed below is the best procedure for converting 3-Phenylbut-1-ene to 3-Phenylbutan-1-ol? OH a. NaOHA b. i. HCl; ii. NaOH CH202 dH30* e.i. BH3; 11. H2O2, NaOH, H20 f. i. Hg(OAc); ii. NaBH4
What is the best route for converting the alcohol to the ether as shown below using a substitution reaction or a sequence of substitution reactions while preserving the steroochemistry at the chiral center? OH OCH a. NaOCHy b.i. PC13; ii. NaOCH ci.HCI; N.CH OH 4. CH3OH Oei. HCI; il NOCH f. LICH3 What reagents is the best choice for achieving the following chemical transformation? 0 ?? no CH; CC1z O a. PC13 b. Cl2, NaOH c. NaCl, H20 Ed. Cl2...
What is the major Organic product from the following sequence of reactions? 1) NaNH2 2) Br W u on ou oh oh oh NH (a) (d) (e ) a. a b.b d. d e. e f. f Arrange the following species in order of increasing nucleophile strength in an SN 2 reaction. h:1-, CH3NH2, CH301- O a. (Weakest nucleophile) CH3NH2 < CH301- <H:1- (Strongest Nucleophile) O b. (Weakest nucleophile) CH3NH2 <H:1- < CH301- (Strongest Nucleophile) OC (Weakest nucleophile) CH301- <h:1-...
Given the reagents listed below, what is the best route for producing the vicinal cyanohydrin shown below starting from 1-methylcyclohexene? Note: The order in which the reagents are added matters. Some of the reagents may not be used. List of reagents: NACN HCN MCPBA (m-chloroperoxybenzoic acid) HBI NaOH CN CH, CH CH CN ОН OH CH CH; (CH MICN OH ОН a. i. HBr; ii. NaCN; iii, NaOH b.i. MCPBA; ii. HCN T c. i. NaCN; ii. NaOH n di...
Given the reagents listed below, what is the best route for producing the vicinal cyanohydrin shown below starting from 1-methylcyclohexene? Note: The order in which the reagents are added matters. Some of the reagents may not be used, List of reagents: NaCN HCN MCPBA (m-chloroperoxybenzoic acid) HB NaOH CN CH .CH CH GICN HOH он MCPBA (m-chloroperoxybenzoic acid) HBr NaOH CN CH CH; CH; o & CN OH ОН a. i. HBr; ii. NaCN; iii. NaOH b.i. MCPBA; ii. HCN...
Testbank, Question 015 Select the best reagents for the reaction below. + enantiomer OH 1) OsO4; 2) NaHSO3, H20 1) Hg(OAC)2, H20; 2) NaBH4 1) RCOZH; 2) H30+ 1) BH3-THF; 2) H2O2, NaOH 1) 03; 2) DMS
In each reaction box, place the best reagent and conditions from the list below. OH NaBH4 in EtoH PC13 Cl2, H20 H2SO4 (conc.) Br2 H20ro4 H202, NaOH, H20 dilute H3O BH3 THF OH
In each case below select the synthetic procedure/s that could be used to carry out the transformation, giving the alcohol shown as the single major product The procedures are: Hydroboration/oxidation: alkene BH3; then H202, OH Oxymercuration: alkene + Hg(OAc)2, H2O; then NaBH4 ОН CH-CHз CH2CH3 CHз CНз Cн-CH-CHCHCHЗ CH3CH2CHCH=CH2 ОН
Which reaction conditions would you use to perform the reaction shown below? HO CHE O 1. BH3, THE 2. H2O2, OH, H20 O 1. Oso 2. NaHSO3 H2O 1.03 2. Zn/H20 or DMS 1. Hg(OAC)2, H20 2. NaBH4