Homework Answers
Please give better ratingAdd Answer to:
complete the reactions bu adding the starting material, reaction
conditions, or all possible products
Ph H...
Complete the following with the correct products, label Zaitsev and Hofmann, and explain why the reaction...
Complete the following with the correct products, label Zaitsev and Hofmann, and explain why the reaction is either regioselective or stereoselective. (6 pts.) D -Br Nahi Complete each of the following reactions by adding the starting material, reaction conditions, or all possible product(s) - label major/minor - Sx2. Sx1, E2 or E1. (33 pts.) (CH3),COK DMF C(CH3) NaOH DMSO CH OH heat Ph H+Br NaOCH, H+CHE Ph DMF SK DMF o (only product)
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash...
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash notation (i.e., as shown in the starting material). If a reaction produces a racemic mixture, show only one of the enantiomers produced. Carefully note the requested reaction mechanism for each reaction. (20 pts) NaOCH3 CH3OH SN2 Br CH3OH SN1 Br NaOCH3 CH3OH E2 Show Zaitsev product Br CH3OH Br E1
Select all the possible reaction conditions that would enable the transformation of the starting material(s) into...
Select all the possible reaction conditions that would enable
the transformation of the starting material(s) into the
product(s).
Question 10 2 pts Select all the possible reaction conditions that would enable the transformation of the starting material(s) into the product(s) CI a) 1-butylamine, pyridine b) work-up a) butyl-1,4-diamine, pyridine b) work-up a) H2SO4 (cat.), pyridine b) work-up a) Pyrrolidine, pyridine b)work-up a) Pyridine b) work-up
Question 10 2 pts Select all the possible reaction conditions that would enable the transformation...
Select all the possible reaction conditions that would enable the transformation of the starting material(s) into...
Select all the possible reaction conditions that would enable
the transformation of the starting material(s) into the
product(s).
Question 2 2 pts Select all the possible reaction conditions that would enable the transformation of the starting material(s) into the product(s) ? OCH3 OH a) H2SO4(cat), CH3OH b) work-up a) PBr3, solvent b)work-up a) NaOH, H2O b) work-up a) H2SO 4(cat), H20 b) work-up a) SOCI2, CH30H b) work-up
Question 2 2 pts Select all the possible reaction conditions that would...
Write the structure of the main product, reaction conditions or starting material for each reaction as the case may be....
Write the structure of the main product, reaction conditions
or starting material for each reaction as the case may be. Remember
to write the product with the appropriate stereochemistry.
5. (1) NaNO,/HC NH, (2) HBF, 6 NH2 NaNO,/HC но Br 7. H2NCH2CH3 pH 4.5 8. OCH3 Hао H*
What starting material is required in order to complete the reaction scheme for the synthesis shown...
What starting material is required in order to complete the reaction scheme for the synthesis shown below? OCH3 1. Na 2. CH₂ Br CH₃ 7 I.NaNO2 / HCI 2. KI Product ? CH3 2 Br KMnO4 H₂o" heat CH3 1. HNO₃ H₂SO4 / heat 2. Sn / HCl 3. NaHCO₃
6. (24 pts) Complete the reactions shown below, remember to show all relevant stereochemistry. For products...
6. (24 pts) Complete the reactions shown below, remember to show all relevant stereochemistry. For products only draw the MAJOR product, if the conditions yield no reaction indicate "no reaction." Alkyl Halide H C Br HỌC CH, NaOCH,CH Br bo o led bono
Please answer in detail. 8 9. Show all possible products (major and minor) for the reactions...
Please answer in detail.
8 9. Show all possible products (major and minor) for the reactions below. Specify if the reaction is stereospecific. NaOH Zсн, ? Br Ph. CH3-CH2-ONa Br Base (KOH) он CH3! H30
S. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s)....
S. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s). Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. C4 CyHO 61 41 Use the provided template сн,он Include a mechanism for the above reaction 4 1 eg HCI High Temp +2 HSOHgSOHo br-t- Br
S. (28 pt.) Complete the following reactions with the correct structures of starting material or...
please show all steps including each mechanism (arrows) and also if SN1 has any rearrangements of...
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
Complete the following with the correct products, label Zaitsev and Hofmann, and explain why the reaction is either regioselective or stereoselective. (6 pts.) D -Br Nahi Complete each of the following reactions by adding the starting material, reaction conditions, or all possible product(s) - label major/minor - Sx2. Sx1, E2 or E1. (33 pts.) (CH3),COK DMF C(CH3) NaOH DMSO CH OH heat Ph H+Br NaOCH, H+CHE Ph DMF SK DMF o (only product)
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash notation (i.e., as shown in the starting material). If a reaction produces a racemic mixture, show only one of the enantiomers produced. Carefully note the requested reaction mechanism for each reaction. (20 pts) NaOCH3 CH3OH SN2 Br CH3OH SN1 Br NaOCH3 CH3OH E2 Show Zaitsev product Br CH3OH Br E1
Select all the possible reaction conditions that would enable
the transformation of the starting material(s) into the
product(s).
Question 10 2 pts Select all the possible reaction conditions that would enable the transformation of the starting material(s) into the product(s) CI a) 1-butylamine, pyridine b) work-up a) butyl-1,4-diamine, pyridine b) work-up a) H2SO4 (cat.), pyridine b) work-up a) Pyrrolidine, pyridine b)work-up a) Pyridine b) work-up
Question 10 2 pts Select all the possible reaction conditions that would enable the transformation...
Select all the possible reaction conditions that would enable
the transformation of the starting material(s) into the
product(s).
Question 2 2 pts Select all the possible reaction conditions that would enable the transformation of the starting material(s) into the product(s) ? OCH3 OH a) H2SO4(cat), CH3OH b) work-up a) PBr3, solvent b)work-up a) NaOH, H2O b) work-up a) H2SO 4(cat), H20 b) work-up a) SOCI2, CH30H b) work-up
Question 2 2 pts Select all the possible reaction conditions that would...
Write the structure of the main product, reaction conditions
or starting material for each reaction as the case may be. Remember
to write the product with the appropriate stereochemistry.
5. (1) NaNO,/HC NH, (2) HBF, 6 NH2 NaNO,/HC но Br 7. H2NCH2CH3 pH 4.5 8. OCH3 Hао H*
What starting material is required in order to complete the reaction scheme for the synthesis shown below? OCH3 1. Na 2. CH₂ Br CH₃ 7 I.NaNO2 / HCI 2. KI Product ? CH3 2 Br KMnO4 H₂o" heat CH3 1. HNO₃ H₂SO4 / heat 2. Sn / HCl 3. NaHCO₃
6. (24 pts) Complete the reactions shown below, remember to show all relevant stereochemistry. For products only draw the MAJOR product, if the conditions yield no reaction indicate "no reaction." Alkyl Halide H C Br HỌC CH, NaOCH,CH Br bo o led bono
Please answer in detail.
8 9. Show all possible products (major and minor) for the reactions below. Specify if the reaction is stereospecific. NaOH Zсн, ? Br Ph. CH3-CH2-ONa Br Base (KOH) он CH3! H30
S. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s). Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. C4 CyHO 61 41 Use the provided template сн,он Include a mechanism for the above reaction 4 1 eg HCI High Temp +2 HSOHgSOHo br-t- Br
S. (28 pt.) Complete the following reactions with the correct structures of starting material or...
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
Most questions answered within 3 hours.
-
A marketing executive who knowingly authorizes a shoddy
defective product to be brought to market is...
asked 2 minutes ago -
Write a psudocode:
1. Define a function called authorize that takes in 2 strings,
uName, and...
asked 7 minutes ago -
What Hall voltage (in mV) is produced by a 0.180 T field applied
across a 2.60...
asked 6 minutes ago -
What mass of ethylene glycol (C2H6O2) must be added to 211.0 g
of water to obtain...
asked 9 minutes ago -
Mary's employer has a defined benefits retirement plan, which
pay 3.2% of her last year's salary...
asked 12 minutes ago -
What are the characteristics and behavior of an ethical
manager?
Explain, in your words, what ethics...
asked 29 minutes ago -
1. Which of the following is NOT an argument that McMahan uses
to show that jus...
asked 50 minutes ago -
A crate slides up a frictionless slope. At the end of 3 seconds
its velocity is...
asked 1 hour ago -
Use the following information to answer the next seven
questions.
Suppose there are three potential states...
asked 1 hour ago -
If we only have interstitial and substitutional diffusion, then
what do we consider the process of...
asked 1 hour ago -
You look at yourself in a shiny 9.6-cm-diameter Christmas tree
ball.
If your face is 21.0...
asked 1 hour ago -
If we were to measure the relaxation time of a muscle after
undergoing tetanus compared to...
asked 1 hour ago