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am trying to figure out the starting materials, solvent, and
reagent to form the product...
what are the starting matrial, solvent, and reagent to use to get 1-phenyl-1-propanol? Grignard Addition VCL...
what are the starting matrial, solvent, and reagent to use to
get 1-phenyl-1-propanol?
Grignard Addition VCL 10-1: Grignard Addition - 1 For this assignment, the target compound that you should synthesize is 1-phenyl-1-propanol. This is an organometallic addition reaction. Examine the product and identify potential bonds that may be formed. Keep in mind the mechanism and the need to quench the reaction with acid to liberate the neutral product. Synthesis Procedures 1. Start Virtual ChemLab and select Grignard Addition -/...
1. Propose a mechanism: Starting material: butyraldehyde Solvent: water Reagent: Potassium Hydroxide(KOH) Final product: 2-ethyl-3-hydroxy-hexanal 2....
1. Propose a mechanism: Starting material: butyraldehyde Solvent: water Reagent: Potassium Hydroxide(KOH) Final product: 2-ethyl-3-hydroxy-hexanal 2. Propose a mechanism: Starting material: Methyl Propionate Solvent: water Reagent: HCl Final product: propionic acid
7. Choose your own adventure.Choose one of the starting materials below, then treat ti with three...
7. Choose your own adventure.Choose one of the starting materials below, then treat ti with three of the reagents listed, showing the expected product after each step. (9 pts) Starting materials Reagents [H+], H2O H+], H20 NaBH4, EtOH 1. LiAlH4 2. H3O+ CH2-PPh3 NaOH(aq), then H30+ SOCl2 DIBAL Br2, hv 1. BH3, THF, 2. H202, NaOH TMSCI, pyridine PBr3 1. NaH 2. CH3CH2Br PCC H2, Pd/C CH3CH2OH Starting material Product 1 Final product Product 2
Which starting matrial, solvent and reagent should I use to get 1-phenyl-1-propanol? Grignard Addition VCL 10-1:...
Which starting matrial, solvent and reagent should I use to
get 1-phenyl-1-propanol?
Grignard Addition VCL 10-1: Grignard Addition - 1 For this assignment, the target compound that you should synthesize is 1-phenyl-1-propanol. This is an organometallic addition reaction. Examine the product and identify potential bonds that may be formed. Keep in mind the mechanism and the need to quench the reaction with acid to liberate the neutral product. Synthesis Procedures 1. Start Virtual ChemLab and select Grignard Addition - /...
1. Provide the appropriate Wittig starting materials used to form the following product. Stereochemistry must be...
1. Provide the appropriate Wittig starting materials used to form the following product. Stereochemistry must be included where appropriate: 1.) Triphenylphosphine 2.) 50% NaOH, H20 2. Provide a synthesis of the following compound using the alkene provided as your only source of carbon. Multiple equivalents of the alkene can be used. You may use triphenylphosphine, and any additional inorganic reagents required as well. You may use any other carbon containing reagent as well, provided that it is not used as...
no explanation needed, I just need the right answer choices. Thank you!! Predict the major organic...
no explanation needed, I just need the right answer choices.
Thank you!!
Predict the major organic product of the following reactions. Assume one equivalent of reagent unless otherwise stated, it's a solvent, oxidizing, or reducing agent. If no reaction will occur, choose E. Be mindful of stereochemistry. Me Me 1. Mgº, THE o Br Me H Me 1 Me 3. H20, HCI Me Y Me Me Me Me Me Me Me HO он Me Me Me Me Predict the major...
I need help with questions 5, 6, & 7. The FTIR and NMR is provided. I...
I need help with questions 5, 6, & 7. The FTIR and NMR is
provided. I also need help creating a reaction mechanism using the
following:
Starting material: 1,7-Dimethyl-heptanedioate
Solvent: Diethyl ether
Reagent: sodium methoxide
Product: 3-oxo-cyclohexane carboxylic acid methyl ester
THANK YOU!!!!!
Ö 11-11: Dieckmann Reaction For this assignment, the target compound that you should synthesize is 2-oxo-cyclohexane carboxylic acid methyl ester.This is an intramolecular carbonyl addition variation. Examine the product and determine which ester is the nucleophile and...
I need help with questions 5, 6, & 7. The FTIR and NMR is provided. I...
I need help with questions 5,
6, & 7. The FTIR and NMR is provided. I also need help creating
a reaction mechanism using the following:
Starting material: methyl acetate.
Solvent: diethyl ether
Reagent: sodium methoxide
Product: methyl acetoacetate
THANK YOU!!!!!
11-8: Claisen Condensation - 1 For this assignment, the target compound that you should synthesize is methyl acetoacetate.This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep...
To carryout a synthesis from my target molecules which is label as #20. I choose p-anisidine...
To carryout a synthesis from my target molecules which is label
as #20. I choose p-anisidine and/or p-toluidine as my "starting
materials" and here is a list of reagents to get to my target
molecules. Can you show me the way what is the correct way to do
synthesis to get to my target molecules.
CH3 ОН , Hood Numbers: 4,12, 20) Reagents: The reagents listed below will be available, stored according to hazard class. Requests for reagents not listed...
how do i calculate the number of moles, theoretical yield, and limiting reagent on the READ...
how do i calculate the number of moles, theoretical yield, and
limiting reagent on the READ ABOUT part? thank you
i need help on READ ABOUT: Calculate the number of moles of
2-methyl-2-butanol and hydrochloric acid (concentrated HCl is 12
M). Based on the balanced equation, determine the limiting reagent
and the theoretical yield of 2-chloride-2-methylbutane.
PREPARATION AND ANALYSIS OF T-AMYL CHLORIDE ОН HCI (conc.) + H2O DISCUSSION: Compounds with good leaving groups often participate in substitution reactions. Two limiting...
what are the starting matrial, solvent, and reagent to use to
get 1-phenyl-1-propanol?
Grignard Addition VCL 10-1: Grignard Addition - 1 For this assignment, the target compound that you should synthesize is 1-phenyl-1-propanol. This is an organometallic addition reaction. Examine the product and identify potential bonds that may be formed. Keep in mind the mechanism and the need to quench the reaction with acid to liberate the neutral product. Synthesis Procedures 1. Start Virtual ChemLab and select Grignard Addition -/...
7. Choose your own adventure.Choose one of the starting materials below, then treat ti with three of the reagents listed, showing the expected product after each step. (9 pts) Starting materials Reagents [H+], H2O H+], H20 NaBH4, EtOH 1. LiAlH4 2. H3O+ CH2-PPh3 NaOH(aq), then H30+ SOCl2 DIBAL Br2, hv 1. BH3, THF, 2. H202, NaOH TMSCI, pyridine PBr3 1. NaH 2. CH3CH2Br PCC H2, Pd/C CH3CH2OH Starting material Product 1 Final product Product 2
Which starting matrial, solvent and reagent should I use to
get 1-phenyl-1-propanol?
Grignard Addition VCL 10-1: Grignard Addition - 1 For this assignment, the target compound that you should synthesize is 1-phenyl-1-propanol. This is an organometallic addition reaction. Examine the product and identify potential bonds that may be formed. Keep in mind the mechanism and the need to quench the reaction with acid to liberate the neutral product. Synthesis Procedures 1. Start Virtual ChemLab and select Grignard Addition - /...
1. Provide the appropriate Wittig starting materials used to form the following product. Stereochemistry must be included where appropriate: 1.) Triphenylphosphine 2.) 50% NaOH, H20 2. Provide a synthesis of the following compound using the alkene provided as your only source of carbon. Multiple equivalents of the alkene can be used. You may use triphenylphosphine, and any additional inorganic reagents required as well. You may use any other carbon containing reagent as well, provided that it is not used as...
no explanation needed, I just need the right answer choices.
Thank you!!
Predict the major organic product of the following reactions. Assume one equivalent of reagent unless otherwise stated, it's a solvent, oxidizing, or reducing agent. If no reaction will occur, choose E. Be mindful of stereochemistry. Me Me 1. Mgº, THE o Br Me H Me 1 Me 3. H20, HCI Me Y Me Me Me Me Me Me Me HO он Me Me Me Me Predict the major...
I need help with questions 5, 6, & 7. The FTIR and NMR is
provided. I also need help creating a reaction mechanism using the
following:
Starting material: 1,7-Dimethyl-heptanedioate
Solvent: Diethyl ether
Reagent: sodium methoxide
Product: 3-oxo-cyclohexane carboxylic acid methyl ester
THANK YOU!!!!!
Ö 11-11: Dieckmann Reaction For this assignment, the target compound that you should synthesize is 2-oxo-cyclohexane carboxylic acid methyl ester.This is an intramolecular carbonyl addition variation. Examine the product and determine which ester is the nucleophile and...
I need help with questions 5,
6, & 7. The FTIR and NMR is provided. I also need help creating
a reaction mechanism using the following:
Starting material: methyl acetate.
Solvent: diethyl ether
Reagent: sodium methoxide
Product: methyl acetoacetate
THANK YOU!!!!!
11-8: Claisen Condensation - 1 For this assignment, the target compound that you should synthesize is methyl acetoacetate.This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep...
To carryout a synthesis from my target molecules which is label
as #20. I choose p-anisidine and/or p-toluidine as my "starting
materials" and here is a list of reagents to get to my target
molecules. Can you show me the way what is the correct way to do
synthesis to get to my target molecules.
CH3 ОН , Hood Numbers: 4,12, 20) Reagents: The reagents listed below will be available, stored according to hazard class. Requests for reagents not listed...
how do i calculate the number of moles, theoretical yield, and
limiting reagent on the READ ABOUT part? thank you
i need help on READ ABOUT: Calculate the number of moles of
2-methyl-2-butanol and hydrochloric acid (concentrated HCl is 12
M). Based on the balanced equation, determine the limiting reagent
and the theoretical yield of 2-chloride-2-methylbutane.
PREPARATION AND ANALYSIS OF T-AMYL CHLORIDE ОН HCI (conc.) + H2O DISCUSSION: Compounds with good leaving groups often participate in substitution reactions. Two limiting...
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