Please show full mechanism with arrows and mechanism name for this multi synthesis problem(C-G)
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Please show full mechanism with arrows and mechanism
name for this multi synthesis problem(C-G)
Me Me...
Please show full mechanism with arrows and mechanism name used in each step. Show all product(s)....
Please show full mechanism with arrows and mechanism
name used in each step. Show all product(s).
Me Nal Me Naci DMF Me HCI Me он НІ DMF
Show the full electron pushing mechanism with arrows for the synthesis of p-bromoaniline from aniline. Show...
Show the full electron pushing mechanism with arrows for the
synthesis of p-bromoaniline from aniline. Show any side
products
NH3 N 'CH3 NH CH HCI, H2O 1) H+, H20 Br2 H3C CH COONa CH COOH 2) 5% NaOH Aniline Acetic anhydride Acetanilide p-bromo acetanilide p-bromoaniline bp 184 oC mp 114 oC mp 166 oC mp 64 oC
Please explain and right in details 145 1. Write a full, complete mechanism for each of...
Please explain and right in details
145 1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: NaOCH, Br a) H2O2 - b) NaOH 0-s- 4.5 'o:
please show each step thanks Show each intermediate (A-C) in the synthesis of the product, which...
please show each step thanks
Show each intermediate (A-C) in the synthesis of the product, which is an important compound used in the or perfumes and fruit fragrances, even though it smells like fresh cut grass! (Annual production of the product is approx. 30 tons.) Also, provide an IUPAC name for the product. (35 poir 1. Bry,hv 1. Br2 2. t-BuOK 2. NaNH, 3. H,O 1. n-Buli 2. 3. H,0 H₂ OH 10 Lindlar's
Show FULL arrow pushing mechanism for this reaction, and explain it step by step. Reagent used...
Show FULL arrow pushing mechanism for this reaction, and explain
it step by step. Reagent used was c) K2CO3, MeOH, room temp., 1 h
(quant.).
(please disregard BOTH arrows on s11, as this only one step of a
multi-step synthesis)
Label all chiral centers on s12 and draw its enantiomer
ОН OH C Y і 0 (97 : 3) Л s11 Л s12
3. Devise a multi-step synthesis of the target molecule from the given starting material. Show all...
3. Devise a multi-step synthesis of the target molecule from the given starting material. Show all necessary reagents and conditions for each step and the product of each step. (7) OH BONUS: Please provide the arrow pushing mechanism of this reaction. Be sure to show a charges and stereochemistry where needed. To receive full credit, what is the name of this reaction? (4) NaOE HOE Br
Please show the arrows on how to achieve the answer. I am getting very confused about...
Please show the arrows on how to achieve the answer. I am
getting very confused about the role of NaOH/heat and NaOH/Br2.
Thanks
42. What reagents are needed to complete the following synthesis? OH A) 1. NaOH / heat, 2. HCl (aq) B) 1. NaOH / Br2, 2. HCl (aq) C) 1. warm conc. KMnO4 /NaOH, 2. HCl (aq) D) 1. Ag(NH3)2OH, 2. HCl (aq)
Please show all mechanism arrows 4. Devise a synthesis for the bromohydrin shown from bromocyclohexane. Multipl...
Please show all mechanism arrows
4. Devise a synthesis for the bromohydrin shown from bromocyclohexane. Multipl are required, and you may use any combination of reagents and chemicals. Br Br OH nd Which compound below would give rise to 5 signals in the proton NMR 5t
please explain How many "curved arrows are needed to describe the mechanism for formation of this...
please explain
How many "curved arrows are needed to describe the mechanism for formation of this intermediate? CH [D] 1 (EJ 2 IA 3 IC) 3 [B] 4 Explanation for your choice (3 pts) How can this transformation be accomplished? OH снен A. Br/CCL B. HYPd-C C.O.CH.OH G. HO/acid D. BryH.0 H. BẠH. E. Zn F.H.O I. H-0./NaOH J. CI HO K. NaH L. mCPBA M. HSO/A N. TsCpy O. KMnO/KOH TAJ H then G P. NaOH [B] O then...
please answer all all do not answer. only show the mechanism for the first one. I...
please answer all all do not answer. only show the mechanism for
the first one.
I give good review.
Worksheet Problem 1(c): Predict the major product of the reaction below, taking substituent directing (and steric) effects into account: DEt C12 FeCl3 CN CMCN (A) (B) (C) (D) Worksheet Problem 1(d): Predict the major product of the reaction below, taking substituent directing (and steric) effects into account: AICI Br (A) (B) (C) (D) Worksheet Problem 2(c): Propose an efficient synthesis for...
Please show full mechanism with arrows and mechanism
name used in each step. Show all product(s).
Me Nal Me Naci DMF Me HCI Me он НІ DMF
Show the full electron pushing mechanism with arrows for the
synthesis of p-bromoaniline from aniline. Show any side
products
NH3 N 'CH3 NH CH HCI, H2O 1) H+, H20 Br2 H3C CH COONa CH COOH 2) 5% NaOH Aniline Acetic anhydride Acetanilide p-bromo acetanilide p-bromoaniline bp 184 oC mp 114 oC mp 166 oC mp 64 oC
Please explain and right in details
145 1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: NaOCH, Br a) H2O2 - b) NaOH 0-s- 4.5 'o:
please show each step thanks
Show each intermediate (A-C) in the synthesis of the product, which is an important compound used in the or perfumes and fruit fragrances, even though it smells like fresh cut grass! (Annual production of the product is approx. 30 tons.) Also, provide an IUPAC name for the product. (35 poir 1. Bry,hv 1. Br2 2. t-BuOK 2. NaNH, 3. H,O 1. n-Buli 2. 3. H,0 H₂ OH 10 Lindlar's
Show FULL arrow pushing mechanism for this reaction, and explain
it step by step. Reagent used was c) K2CO3, MeOH, room temp., 1 h
(quant.).
(please disregard BOTH arrows on s11, as this only one step of a
multi-step synthesis)
Label all chiral centers on s12 and draw its enantiomer
ОН OH C Y і 0 (97 : 3) Л s11 Л s12
3. Devise a multi-step synthesis of the target molecule from the given starting material. Show all necessary reagents and conditions for each step and the product of each step. (7) OH BONUS: Please provide the arrow pushing mechanism of this reaction. Be sure to show a charges and stereochemistry where needed. To receive full credit, what is the name of this reaction? (4) NaOE HOE Br
Please show the arrows on how to achieve the answer. I am
getting very confused about the role of NaOH/heat and NaOH/Br2.
Thanks
42. What reagents are needed to complete the following synthesis? OH A) 1. NaOH / heat, 2. HCl (aq) B) 1. NaOH / Br2, 2. HCl (aq) C) 1. warm conc. KMnO4 /NaOH, 2. HCl (aq) D) 1. Ag(NH3)2OH, 2. HCl (aq)
Please show all mechanism arrows
4. Devise a synthesis for the bromohydrin shown from bromocyclohexane. Multipl are required, and you may use any combination of reagents and chemicals. Br Br OH nd Which compound below would give rise to 5 signals in the proton NMR 5t
please explain
How many "curved arrows are needed to describe the mechanism for formation of this intermediate? CH [D] 1 (EJ 2 IA 3 IC) 3 [B] 4 Explanation for your choice (3 pts) How can this transformation be accomplished? OH снен A. Br/CCL B. HYPd-C C.O.CH.OH G. HO/acid D. BryH.0 H. BẠH. E. Zn F.H.O I. H-0./NaOH J. CI HO K. NaH L. mCPBA M. HSO/A N. TsCpy O. KMnO/KOH TAJ H then G P. NaOH [B] O then...
please answer all all do not answer. only show the mechanism for
the first one.
I give good review.
Worksheet Problem 1(c): Predict the major product of the reaction below, taking substituent directing (and steric) effects into account: DEt C12 FeCl3 CN CMCN (A) (B) (C) (D) Worksheet Problem 1(d): Predict the major product of the reaction below, taking substituent directing (and steric) effects into account: AICI Br (A) (B) (C) (D) Worksheet Problem 2(c): Propose an efficient synthesis for...
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