Homework Answers
1) starting material is 1-propanol (an alcohol)
2) the product is an ether [ propylbutyl ether is the common name and 1-propoxybutane is the IUPAC name]
3) see pic.
4)i)sodium metal
ii) sodium propoxide with n-butylether 
Add Answer to:
1. What is the starting material?
2. What is the product?
3. What is the step...
Devise a 5-step synthesis of the product from the starting material and reagents provided. 1. reagent...
Devise a 5-step synthesis of the product from the starting material and reagents provided. 1. reagent 1 2. reagent 2 "NH2 3. reagent 3 4. reagent 4 5. reagent 5
Devise a 4-step synthesis of the product from the starting material shown. 1. reagent 1 2....
Devise a 4-step synthesis of the product from the starting material shown. 1. reagent 1 2. reagent 2 3. reagent 3 4. reagent 4 HOT Identify reagent 1. Identify reagent 2. Identify reagent 3. Identify reagent 4.
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
Draw the missing major organic product(s), starting material(s), or reagents for each of the following reactions...
Draw the missing major organic product(s), starting
material(s), or reagents for each of the following reactions (DO
NOT WRITE +EN AS A PRODUCT (ie draw everything out!)! And remember
stereo and regiochemistry.) Assume reagents are in excess unless
otherwise indicated. **To make things simple, I indicated what is
needed for each section! Please don't just put the answers, but
explanations as well on why. Thanks!
a) draw the starting material for this reaction.
b) draw the product for this reaction....
Propose an efficient 2-step synthesis for the following ether from an alcohol starting material. Draw the alcohol start...
Propose an efficient 2-step synthesis for the following ether
from an alcohol starting material. Draw the alcohol starting
material and select the best reagents from the given
toolbox.
Choices for toolbox 1 and 2: NaH, CH3CH2CHBrCH3, CH3CH2Br,
NaOH/H2O
Propose an efficient 2-step synthesis for the following ether from an alcohol starting material. Draw the alcohol starting material and select the best reagents from the given toolbox 1.Select answer Select answer 2. I
4-Suggest a synthesis of the target molecule from the indicated starting material. More than one step...
4-Suggest a synthesis of the target molecule from the indicated starting material. More than one step will be required. For each step of your reaction sequence, show reagents used and product(s) formed. No curved arrows are required.(6 Marks)
Specify both the alcohol starting material and the reagents you would use in each step in...
Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3 Cl CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3.1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LiAlH4 f. PBr k. CH3 CH2CH2 then H3O L CsHsMgBr (phenylmagnesium bromide); then H3o m. (CHs)2CHMgBr: then Hgo d. HBr i. CH, MgBr, then Ho .Dess-Martin periodinane (DMP) e....
4-Suggest a synthesis of the target molecule from the indicated starting material. More than one step...
4-Suggest a synthesis of the target molecule from the indicated starting material. More than one step will be required. For each step of your reaction sequence, show reagents used and product(s) formed. No curved arrows are required. of N=0 O=0
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
le chatelier experimen Thursday). 1. What starting material and reagents are needed for the following multi-s...
le
chatelier experimen
Thursday). 1. What starting material and reagents are needed for the following multi-step synthesis (HINT: aldol reactions work best when the starting material can only form one enolate)? 5 он о D. NaOH, H2O, Heat F. HO E. NaOH, H2O G. LDA Starting Material: Reagents: 2. LDA is a strong, sterically hindered base and will form the enolate. Sodium hydride is a weak base and will form the _ - enolate. Kinetic enolates are the stable and...
Devise a 5-step synthesis of the product from the starting material and reagents provided. 1. reagent 1 2. reagent 2 "NH2 3. reagent 3 4. reagent 4 5. reagent 5
Devise a 4-step synthesis of the product from the starting material shown. 1. reagent 1 2. reagent 2 3. reagent 3 4. reagent 4 HOT Identify reagent 1. Identify reagent 2. Identify reagent 3. Identify reagent 4.
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
Draw the missing major organic product(s), starting
material(s), or reagents for each of the following reactions (DO
NOT WRITE +EN AS A PRODUCT (ie draw everything out!)! And remember
stereo and regiochemistry.) Assume reagents are in excess unless
otherwise indicated. **To make things simple, I indicated what is
needed for each section! Please don't just put the answers, but
explanations as well on why. Thanks!
a) draw the starting material for this reaction.
b) draw the product for this reaction....
Propose an efficient 2-step synthesis for the following ether
from an alcohol starting material. Draw the alcohol starting
material and select the best reagents from the given
toolbox.
Choices for toolbox 1 and 2: NaH, CH3CH2CHBrCH3, CH3CH2Br,
NaOH/H2O
Propose an efficient 2-step synthesis for the following ether from an alcohol starting material. Draw the alcohol starting material and select the best reagents from the given toolbox 1.Select answer Select answer 2. I
4-Suggest a synthesis of the target molecule from the indicated starting material. More than one step will be required. For each step of your reaction sequence, show reagents used and product(s) formed. No curved arrows are required.(6 Marks)
Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3 Cl CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3.1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LiAlH4 f. PBr k. CH3 CH2CH2 then H3O L CsHsMgBr (phenylmagnesium bromide); then H3o m. (CHs)2CHMgBr: then Hgo d. HBr i. CH, MgBr, then Ho .Dess-Martin periodinane (DMP) e....
4-Suggest a synthesis of the target molecule from the indicated starting material. More than one step will be required. For each step of your reaction sequence, show reagents used and product(s) formed. No curved arrows are required. of N=0 O=0
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
le
chatelier experimen
Thursday). 1. What starting material and reagents are needed for the following multi-step synthesis (HINT: aldol reactions work best when the starting material can only form one enolate)? 5 он о D. NaOH, H2O, Heat F. HO E. NaOH, H2O G. LDA Starting Material: Reagents: 2. LDA is a strong, sterically hindered base and will form the enolate. Sodium hydride is a weak base and will form the _ - enolate. Kinetic enolates are the stable and...
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