Help!!Homework Answers
Step 1:HBr
Step 2:NaN3
Step 3:H2, Pd/C
In the first step, HBr adds across the double bond
In the second step, N3- substitutes Br-
In the third step, N2 gets eliminated. H2, Pd/C reduces the azide to amine
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3 steps ŅH2 REAGENT BANK A. SOCI2 D. HBO G. NaCN J. Brą, NaOH, H2O...
Propose a feasible synthesis for the following compound. The starting material is already given, you just...
Propose a feasible synthesis for the following compound. The starting material is already given, you just need to supply the next steps using the reagent bank. Assume aqueous work-up is applied when needed. • Assume you have enough equivalence for complete transformation, so you DO NOT need to repeat the letters or indicate the # of equivalence you need. . If the reagent you need is not in the bank, write NONE. • The number of steps you need is...
Question 20 15 pts OH A) HBO K) Cl2, hv B) NaOH, H2O L) SOCI2 C)...
Question 20 15 pts OH A) HBO K) Cl2, hv B) NaOH, H2O L) SOCI2 C) CH3COONa, DMF M) LIAIHA, THE D) CH3CH2CH2CH2MgBr, ether N) NaBH4, CH3CH2OH E) CH3CH2MgBr, ether O) CH3CH2OH, H2SO4 F) CH3CH2Li, ether P) CH3CH2ON, CH3OH G) Croz, H2SO4, H20 Q) H3O+ H) PCC, CH2Cl2 R) PBr3 1) Brą, hv S) H2, Pd J) heat T) CH3CH2CH2CH2OH, heat U) H20, H2SO4 Look at the given synthesis and the provided reagents. Fill in the blanks with the single...
Indicate if the given statements are TRUE or FALSE regarding Hell Volhard Zelinski reaction 1. The...
Indicate if the given statements are TRUE or FALSE regarding Hell Volhard Zelinski reaction 1. The reaction involves nucleophilic acyl substitution as well as alpha substitution. II. Bra facilitates the formation of the acid bromide. III. Hell Volhard Zelinski can also be done using acetic acid as the catalyst. IV. Br2 acts as the electrophile in the a-bromination step. Propose a feasible synthesis for the following compound. The starting material is already given, you just need to supply the next...
Specify the reagent you would use in each step of the following synthesis: step 1 step...
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 step 2 Reagents Available a. LIAIHA f. PBr3 b. H2SO4 c. HCI d. HBO e. SOC2 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CH.MgBr (phenylmagnesium bromide) h. Nah m. (CH3)2CHMgBr 1. NaOH n. Croz J. CH3MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 Submit Answer Retry Entire Group 9 more group...
These synthesis reactions are kicking my butt and I'd appreciate some help with how to go...
These synthesis reactions are kicking my butt and I'd
appreciate some help with how to go about answering these, or if
anyone has any pointers on how to look at these types of problems.
Thank you!
Specify the reagent you would use in each step of the following synthesis: CH3 H3C CH3 step 1 step 2 H3C CH3 Reagents Available a. LiAIHA b. H2SO4 c. HCI f. PBr3 K. CH3CH2MgBr g. Dess-Martin periodinane (DMP) L. CH MgBr (phenylmagnesium bromide) h....
Specify the reagent you would use in each step of the following synthesis: I step 1...
Specify the reagent you would use in each step of the following synthesis: I step 1 step 2 Reagents Available a. LiAIH4 b. H2SO4 c. HCI f. PBrz k. CH2CH2MgBr g. Dess-Martin periodinane (DMP) 1. CH5MgBr (phenylmagnesium bromide) h. NaH m. (CH3)2CHMgBr i. NaOH n. Croz j. CH3MgBr d. HBr e. SOCI2 Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2
please write the steps needed to get this product. A NaBH4/H:0 S KMnO4 HNO3 H2SO4 K...
please write the steps needed to get this product.
A NaBH4/H:0 S KMnO4 HNO3 H2SO4 K HNO3 H2SO4 B LiAlH4/H:07 T CH3MgBr/H:0* U 1. LDA/ 2. CH Br C Dess-Martin L Nal D CrOz/H:07 M H3PO4 V NaCN E H/Pd N Bry/FeBr3 W NH 0 CH:COCI/AICI: X CH3NH2 P CH:CH-CT/AICI: Y SOCI: F SnCl/H30* 1. Hg(OAc)2, H2O/THF G 2. NaBHA HH2SO4, H2O, HgSO4 1. BH3, THF 2. H2O2, OH Q H3O+/H20 Z CH OH R KOH O CHICHI CH3CH CH:CH-C-OH...
Specify the reagent you would use in each step of the following synthesis: Specify the reagent...
Specify the reagent you would use in each step of the following
synthesis:
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From the table of available reagents select the one(s) you would use to convert butanoic acid...
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• Provide a feasible multi-step synthesis for the following transformation • Write the steps using UPPERCASE...
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Propose a feasible synthesis for the following compound. The starting material is already given, you just need to supply the next steps using the reagent bank. Assume aqueous work-up is applied when needed. • Assume you have enough equivalence for complete transformation, so you DO NOT need to repeat the letters or indicate the # of equivalence you need. . If the reagent you need is not in the bank, write NONE. • The number of steps you need is...
Question 20 15 pts OH A) HBO K) Cl2, hv B) NaOH, H2O L) SOCI2 C) CH3COONa, DMF M) LIAIHA, THE D) CH3CH2CH2CH2MgBr, ether N) NaBH4, CH3CH2OH E) CH3CH2MgBr, ether O) CH3CH2OH, H2SO4 F) CH3CH2Li, ether P) CH3CH2ON, CH3OH G) Croz, H2SO4, H20 Q) H3O+ H) PCC, CH2Cl2 R) PBr3 1) Brą, hv S) H2, Pd J) heat T) CH3CH2CH2CH2OH, heat U) H20, H2SO4 Look at the given synthesis and the provided reagents. Fill in the blanks with the single...
Indicate if the given statements are TRUE or FALSE regarding Hell Volhard Zelinski reaction 1. The reaction involves nucleophilic acyl substitution as well as alpha substitution. II. Bra facilitates the formation of the acid bromide. III. Hell Volhard Zelinski can also be done using acetic acid as the catalyst. IV. Br2 acts as the electrophile in the a-bromination step. Propose a feasible synthesis for the following compound. The starting material is already given, you just need to supply the next...
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 step 2 Reagents Available a. LIAIHA f. PBr3 b. H2SO4 c. HCI d. HBO e. SOC2 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CH.MgBr (phenylmagnesium bromide) h. Nah m. (CH3)2CHMgBr 1. NaOH n. Croz J. CH3MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 Submit Answer Retry Entire Group 9 more group...
These synthesis reactions are kicking my butt and I'd
appreciate some help with how to go about answering these, or if
anyone has any pointers on how to look at these types of problems.
Thank you!
Specify the reagent you would use in each step of the following synthesis: CH3 H3C CH3 step 1 step 2 H3C CH3 Reagents Available a. LiAIHA b. H2SO4 c. HCI f. PBr3 K. CH3CH2MgBr g. Dess-Martin periodinane (DMP) L. CH MgBr (phenylmagnesium bromide) h....
Specify the reagent you would use in each step of the following synthesis: I step 1 step 2 Reagents Available a. LiAIH4 b. H2SO4 c. HCI f. PBrz k. CH2CH2MgBr g. Dess-Martin periodinane (DMP) 1. CH5MgBr (phenylmagnesium bromide) h. NaH m. (CH3)2CHMgBr i. NaOH n. Croz j. CH3MgBr d. HBr e. SOCI2 Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2
please write the steps needed to get this product.
A NaBH4/H:0 S KMnO4 HNO3 H2SO4 K HNO3 H2SO4 B LiAlH4/H:07 T CH3MgBr/H:0* U 1. LDA/ 2. CH Br C Dess-Martin L Nal D CrOz/H:07 M H3PO4 V NaCN E H/Pd N Bry/FeBr3 W NH 0 CH:COCI/AICI: X CH3NH2 P CH:CH-CT/AICI: Y SOCI: F SnCl/H30* 1. Hg(OAc)2, H2O/THF G 2. NaBHA HH2SO4, H2O, HgSO4 1. BH3, THF 2. H2O2, OH Q H3O+/H20 Z CH OH R KOH O CHICHI CH3CH CH:CH-C-OH...
Specify the reagent you would use in each step of the following
synthesis:
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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....
• Provide a feasible multi-step synthesis for the following transformation • Write the steps using UPPERCASE letters in the space provided. • If you need 2 or more equivalence of the same reagent for the step, then write the number of equivalence after the letter, for example A2 ans 2 equivalence of A for that step. • Write NONE in the space if your route is shorter than the indicated number of steps. • Assume a mild acid aqueous workup...
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