1) For the ester below, draw
the structure of the two compounds needed to make the ester and
give the IUPAC name for each.
2) Draw the product/s of the basic hydrolysis of the above ester.
Homework Answers
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1) For the ester below, draw
the structure of the two compounds needed to make the...
Question 1 The ester shown below undergoes hydrolysis to give a carboxylic acid and an alcohol....
Question 1 The ester shown below undergoes hydrolysis to give a carboxylic acid and an alcohol. H30*, H20 ? Provide an IUPAC name for the carboxylic acid that is produced. H BI U A A IX Ex'x, SE TTT12pt Paragraph The ester shown below undergoes hydrolysis to give a carboxylic acid and an alcohol. H30 H2O ? Provide an IUPAC name for the alcohol that is produced. HT BT U A T =
iupac name 1. Give an acceptable IUPAC name for these two compounds. 2. Provide the structure...
iupac name
1. Give an acceptable IUPAC name for these two compounds. 2. Provide the structure of all intermediates and all products 1-14.
. 1) Draw ChemSketch or hand-drawn and name the posible aldehyde and ketone Isomers with CHO...
. 1) Draw ChemSketch or hand-drawn and name the posible aldehyde and ketone Isomers with CHO molecular formula 2 Based on your textbook, show the vidation reaction of each isomer. If there is no reaction, type R . for the following compounds 1. Provide molecular formula 2. Provide IUPAC 3. Show addition of hydrogen reaction draw structures of the products and provide IUPAC name for the products O a 0 1) Draw (ChemSketch or hand-drawn) and name all the possible...
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Gi...
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Give IUPAC name for the following structure. 3) For each reaction below, indicate which starting material is the Nucleophile and which is the Electrophile. Show arrows to demonstrate how the transformation occurs. →^_^tts a Porto ~ onde gi 4) Draw a mechanism for the conversion of the shown starting material to the corresponding product. 5) In the transformation below, a starting material is treated with HCl to form...
3/4 d) Draw the structure of the MINOR product below. No mechanism needed here. (2 pts)...
3/4 d) Draw the structure of the MINOR product below. No mechanism needed here. (2 pts) 7) Draw the mechanism of the elimination reaction below (6 pts) EN (1 pt) b) What is the name of the specific mechanism of the reaction? c) What is being eliminated in the reaction? (2 pts) 8) A molecule in the conformation shown below undergoes the same type of elimination reaction as the previous problem. Draw the product of the reaction in full line...
1. Name the following compounds, IUPAC or Common. ин H₂C CH₂ 2. Draw the structure of...
1. Name the following compounds, IUPAC or Common. ин H₂C CH₂ 2. Draw the structure of the following compounds. a. 3-methyl-3phenylbutanal
owing compounds are "potential' targets for either the malonic ester or the aceto acetic ester synthesis?...
owing compounds are "potential' targets for either the malonic ester or the aceto acetic ester synthesis? Circle them. For each of these, draw the structure(s) of the alkylating agents and structure(s) of the alkylating agents and indicate if the compound could be made efficiently by this method. OH
1. Draw out the missing structure or provide an IUPAC name for each part below (1...
1. Draw out the missing structure or provide an IUPAC name for each part below (1 pt each, 2 pts total): b) Structure: CH3 Name: a) Name: 2-hydroxybenzoic acid Structure:
Draw the 3-D structures for the two compounds given below. For molecule A, draw the chair...
Draw the 3-D structures for the two compounds given below. For molecule A, draw the chair form, determine the number of chiral carbons and the absolute configuration for all of the chiral carbons. For molecule B, determine the number of stereoisomers, draw the 3-D structure of the 2S, 3R, 5S form of the molecule and give the correct name. Importantly, "place appropriate R or S symbols within the immediately proximity of the appropriate chiral carbon center and place your answers...
Which of the following compounds are "potenti acetic ester synthesis? ollowing compounds are "potential' targets for...
Which of the following compounds are "potenti acetic ester synthesis? ollowing compounds are "potential' targets for either the malonic ester or the aceto m. For each of these, draw the structure(s) of the alkylating agents and indicate if the compound could be made efficiently by this method. o
Question 1 The ester shown below undergoes hydrolysis to give a carboxylic acid and an alcohol. H30*, H20 ? Provide an IUPAC name for the carboxylic acid that is produced. H BI U A A IX Ex'x, SE TTT12pt Paragraph The ester shown below undergoes hydrolysis to give a carboxylic acid and an alcohol. H30 H2O ? Provide an IUPAC name for the alcohol that is produced. HT BT U A T =
iupac name
1. Give an acceptable IUPAC name for these two compounds. 2. Provide the structure of all intermediates and all products 1-14.
. 1) Draw ChemSketch or hand-drawn and name the posible aldehyde and ketone Isomers with CHO molecular formula 2 Based on your textbook, show the vidation reaction of each isomer. If there is no reaction, type R . for the following compounds 1. Provide molecular formula 2. Provide IUPAC 3. Show addition of hydrogen reaction draw structures of the products and provide IUPAC name for the products O a 0 1) Draw (ChemSketch or hand-drawn) and name all the possible...
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Give IUPAC name for the following structure. 3) For each reaction below, indicate which starting material is the Nucleophile and which is the Electrophile. Show arrows to demonstrate how the transformation occurs. →^_^tts a Porto ~ onde gi 4) Draw a mechanism for the conversion of the shown starting material to the corresponding product. 5) In the transformation below, a starting material is treated with HCl to form...
3/4 d) Draw the structure of the MINOR product below. No mechanism needed here. (2 pts) 7) Draw the mechanism of the elimination reaction below (6 pts) EN (1 pt) b) What is the name of the specific mechanism of the reaction? c) What is being eliminated in the reaction? (2 pts) 8) A molecule in the conformation shown below undergoes the same type of elimination reaction as the previous problem. Draw the product of the reaction in full line...
1. Name the following compounds, IUPAC or Common. ин H₂C CH₂ 2. Draw the structure of the following compounds. a. 3-methyl-3phenylbutanal
owing compounds are "potential' targets for either the malonic ester or the aceto acetic ester synthesis? Circle them. For each of these, draw the structure(s) of the alkylating agents and structure(s) of the alkylating agents and indicate if the compound could be made efficiently by this method. OH
1. Draw out the missing structure or provide an IUPAC name for each part below (1 pt each, 2 pts total): b) Structure: CH3 Name: a) Name: 2-hydroxybenzoic acid Structure:
Draw the 3-D structures for the two compounds given below. For molecule A, draw the chair form, determine the number of chiral carbons and the absolute configuration for all of the chiral carbons. For molecule B, determine the number of stereoisomers, draw the 3-D structure of the 2S, 3R, 5S form of the molecule and give the correct name. Importantly, "place appropriate R or S symbols within the immediately proximity of the appropriate chiral carbon center and place your answers...
Which of the following compounds are "potenti acetic ester synthesis? ollowing compounds are "potential' targets for either the malonic ester or the aceto m. For each of these, draw the structure(s) of the alkylating agents and indicate if the compound could be made efficiently by this method. o
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