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[References] From the table of available reagents select the one(s) you would use to convert cyclohexanone...
Select the reagents you would use to accomplish the syntheses shown below in no more than...
Select the reagents you would use to accomplish the syntheses shown below in no more than the number of steps specified. List the letters of the reagents in the order that they are used; example: fa. Reagents Available a. HBr b. PBr3 C. (CH3CH2CH2CH2)2Culi f. CH31 g. Hg(OAC)2, H2O, THF; then NaBH4 h. Cl2, light d. (CH3)2Culi I. KOH j. NBS (N-bromosuccinimide) e. BH3, THF; then H202, OH - он CH3 Use 2 steps: V - M Use 3 steps:
Select reagents from the table to show how you would carry out this transformation. If more...
Select reagents from the table to show how you would carry out
this transformation. If more than one route exists, use the one
that requires the fewest steps; in no case will more than 3 steps
be required.
Enter your selection as a series of letters for the reagents in the
order that you wish to use them, i.e. fca.
? CH2 COOH H₃C H3C a. Reagents HBr b. Mg, ether C. CO2, ether then H307 d. BH3, THF then...
From the table of available reagents select the one(s) you would use to convert 1-phenylethanol to...
From the table of available reagents select the one(s) you would use to convert 1-phenylethanol to phenylepoxyethane Reagents available CH_3Br HCI Hg(OCOCF_3)_2 , (CH_3)_2C=CH_2; then NaBH_4 (H_2N)_2C=S; then ^- OH, H_2O H_3O^+ NaH PBr_3 POCI_3, pyridine (CH_3)_3COH
From the table of available reagents, select the one(s) you would use to convert toluene (shown...
From the table of available reagents, select the one(s) you would use to convert toluene (shown above) to each of the following products: (Use the minimum number of steps; in no ease arc more than six steps necessary. List reagents by letter in the order that they are used (example: fa). If an acid workup is required, for example after a Grignard reaction, it must be specified.)
From the table of available reagents select the one(s) you would use to convert butanoic acid...
From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a normal aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) Reagents Available a. benzene/AlCl3 d. H2O, H2SO4 g. LiAlH b....
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the...
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the reagent list handout Step 1 Step 2 Step 3 OH Alkyl Halides (X = CI, Br or 1) and Acyl chlorides: Assume Allig 15 present, if needed CIP CU CH3X X CI E A B EE Ketones. Aldehydes and Epoxides: Assume "then H20" is included if a protonation step is needed F A A K 0 MN Р Grignard, Wittig and Organocuprate Reagents: Assume...
From the table of available reagents select the one(s) you would use to accomplish the transformations...
From the table of available reagents select the one(s) you would use to accomplish the transformations shown below. Use the minimum number of steps: in no case are more than two steps necessary. List reagents by letter in the order that they are used: example: fa.
Help please From the table of available reagents below, select the one(s) you would use to...
Help please
From the table of available reagents below, select the one(s) you would use to accomplish the following conversions. Use the minimum number of steps. List the reagents in order used. No more than 4 steps are necessary. 1-hexyne to 2-methoxyhexane _____ cis-1-methoxy-4-methylcyclohexane to trans-1-bromo-4-methylcyclohexane _____Reagents available a. BH_3, THF: then H_2O_2, ^-OH b. Br_2 c. Hg(OCOCF_3)_2, CH_3CH_2OH: then NaBH_4 d. Hg(OCOCF_3)_2, CH_3OH: then NaBH_4 e. HI, H_2O f: H_2, Lindlar catalyst g. NaH h. ^-OH, H_2O i. ^-OCH_3,...
From the table of available reagents select the one(s) you would use to convert butanoic acid...
From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: f. NOTE: Assume that a normal aqueous (or mild acid) workup follows cach reaction, you do not need to add reagents for the workup.) Reagents Available a benzene/AlCl3 d. H2O, H,804 9. LIAIH 1....
References From the lists of available reagents select the one(s) you would use to in a...
References From the lists of available reagents select the one(s) you would use to in a preparation of acetophenone (phenyl methyl katone) from methylberate (In no case are more than three steps necessary.) . SOCH Reagents Available a CH,COCI, AICI d. CH CHO g. Mg b. (CH3)2Culi e. Ho(OA), H,Othen NaBH, h. NaOH, H, C. CH, MgBr, then H30* . KMnO, H2O 1. Dess-Martin periodinane List reagents by letter in the order that they are used; example: la Reagents used:...
Select the reagents you would use to accomplish the syntheses shown below in no more than the number of steps specified. List the letters of the reagents in the order that they are used; example: fa. Reagents Available a. HBr b. PBr3 C. (CH3CH2CH2CH2)2Culi f. CH31 g. Hg(OAC)2, H2O, THF; then NaBH4 h. Cl2, light d. (CH3)2Culi I. KOH j. NBS (N-bromosuccinimide) e. BH3, THF; then H202, OH - он CH3 Use 2 steps: V - M Use 3 steps:
Select reagents from the table to show how you would carry out
this transformation. If more than one route exists, use the one
that requires the fewest steps; in no case will more than 3 steps
be required.
Enter your selection as a series of letters for the reagents in the
order that you wish to use them, i.e. fca.
? CH2 COOH H₃C H3C a. Reagents HBr b. Mg, ether C. CO2, ether then H307 d. BH3, THF then...
From the table of available reagents select the one(s) you would use to convert 1-phenylethanol to phenylepoxyethane Reagents available CH_3Br HCI Hg(OCOCF_3)_2 , (CH_3)_2C=CH_2; then NaBH_4 (H_2N)_2C=S; then ^- OH, H_2O H_3O^+ NaH PBr_3 POCI_3, pyridine (CH_3)_3COH
From the table of available reagents, select the one(s) you would use to convert toluene (shown above) to each of the following products: (Use the minimum number of steps; in no ease arc more than six steps necessary. List reagents by letter in the order that they are used (example: fa). If an acid workup is required, for example after a Grignard reaction, it must be specified.)
From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a normal aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) Reagents Available a. benzene/AlCl3 d. H2O, H2SO4 g. LiAlH b....
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the reagent list handout Step 1 Step 2 Step 3 OH Alkyl Halides (X = CI, Br or 1) and Acyl chlorides: Assume Allig 15 present, if needed CIP CU CH3X X CI E A B EE Ketones. Aldehydes and Epoxides: Assume "then H20" is included if a protonation step is needed F A A K 0 MN Р Grignard, Wittig and Organocuprate Reagents: Assume...
From the table of available reagents select the one(s) you would use to accomplish the transformations shown below. Use the minimum number of steps: in no case are more than two steps necessary. List reagents by letter in the order that they are used: example: fa.
Help please
From the table of available reagents below, select the one(s) you would use to accomplish the following conversions. Use the minimum number of steps. List the reagents in order used. No more than 4 steps are necessary. 1-hexyne to 2-methoxyhexane _____ cis-1-methoxy-4-methylcyclohexane to trans-1-bromo-4-methylcyclohexane _____Reagents available a. BH_3, THF: then H_2O_2, ^-OH b. Br_2 c. Hg(OCOCF_3)_2, CH_3CH_2OH: then NaBH_4 d. Hg(OCOCF_3)_2, CH_3OH: then NaBH_4 e. HI, H_2O f: H_2, Lindlar catalyst g. NaH h. ^-OH, H_2O i. ^-OCH_3,...
From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: f. NOTE: Assume that a normal aqueous (or mild acid) workup follows cach reaction, you do not need to add reagents for the workup.) Reagents Available a benzene/AlCl3 d. H2O, H,804 9. LIAIH 1....
References From the lists of available reagents select the one(s) you would use to in a preparation of acetophenone (phenyl methyl katone) from methylberate (In no case are more than three steps necessary.) . SOCH Reagents Available a CH,COCI, AICI d. CH CHO g. Mg b. (CH3)2Culi e. Ho(OA), H,Othen NaBH, h. NaOH, H, C. CH, MgBr, then H30* . KMnO, H2O 1. Dess-Martin periodinane List reagents by letter in the order that they are used; example: la Reagents used:...
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