Homework Answers
The reaction mechanism for the product formation is shown below with detail energy profile diagram .
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organic chem, i like your answer immediately
11. Provide an electron-pushing mechanism and an energy diagram...
Draw the SN1 mechanism of the reaction between (R)-3-methylhexane and ethanol. Show lone pairs, electron pushing...
Draw the SN1 mechanism of the reaction between (R)-3-methylhexane
and ethanol. Show lone pairs, electron pushing arrows, 3-D view to
reflect appropriate stereochemistry, reactants,intermediates, and
products. name the product. draw and completely label a reaction
energy diagram corresponding to the mechanism you have drawn.
B. Draw the Snl mechanism of the reaction between (R)-3-bromo-3-methylhexane and ethanol. Show lone pairs, electron pushing arrows, 3-D view to reflect appropriate stereochemistry, reactants, intermediates, and products. You do not have to show transition states....
organic chem, i like your answer immediately 3. A compound with molecular formula of C4H8O2 has...
organic chem, i like your answer immediately
3. A compound with molecular formula of C4H8O2 has one singlet H-NMR peak at 8 3.7 ppm. This compound has a strong IR absorption at 1122 cm!. There is no carbonyl group in this compound. What is the structure of this compound? A. B. C D. 3 1
answer all parts Draw the mechanism (electron pushing and main organic product) for the first step...
answer all parts
Draw the mechanism (electron pushing and main organic product) for the first step of this Kolbe-Schmitt reaction. The Kolbe-Schmitt reaction adds a carboxyl group ortho to the hydroxyl group of phenol. After acidification, salicylic acid is produced. он 1) NaOH OH 2) CO, (100 atm, 125°C) 3) H0 DO A ¢ % o Ć . I I O Z o os Draw the starting material and electron pushing arrows for the third step of this Kolbe-Schmitt reaction....
2. (a) (i) Draw an arrow-pushing mechanism that illustrates the electron flow in the acid-base reaction...
2. (a) (i) Draw an arrow-pushing mechanism that illustrates the electron flow in the acid-base reaction below. Use the structures shown below in your arrow-pushing mechanism. (4pts for correct mechanism). (ii) Using pKa values indicated in Table 1.8 (round to nearest whole number) and estimate the equilibrium constant for this reaction (Keq). Show work which led to this value. (3pts for work, 1pt for correct Keq indicated). (iii) Draw a base (assuming the same acid provided below) that would reverse...
I need help with this homework. I've been sick and out of class and don't know...
I need help with this homework. I've been sick and out of
class and don't know how to do it!! :(
1. Below is a nanodragster...
... wm ve Serected at random for grading, but a full answer key will be posted to Blackboard. 1. Below is a nanodragster. YES, we can make machines-cars, even at the nano-scale, the sizes of molecules. This little nanodragster has some nifty features. Its chassis is rigid like the chassis of a real car....
How to solve alkene and alkyne reactions - Merdanym i Act antalyzod Hrdian ca Come Lazarmistry...
How to solve alkene and alkyne reactions
- Merdanym i Act antalyzod Hrdian ca Come Lazarmistry I V WORKSHOP #9 Alkenes, Alkynes, Reactions 1. Give a reasonable mechanism for the following reaction. Clearly show intermediates and show the movement of electron pairs with curved arrows. all сна H20. (H2SO4) H₃C CH₂ нас он H3CX сна 2. The addition of HBr to 2-methylpropene can, in principle, give either 1-bromo-2- methylpropane or 2-bromo-2-methylpropane. In reality, only the latter is formed. Show mechanisms...
YOU MUST ANSWER THE FOLLOWING QUESTIONS ON YOUR OWN PRIOR TO CLASS REVIEW! 1. Label the...
YOU MUST ANSWER THE FOLLOWING QUESTIONS ON YOUR OWN PRIOR TO CLASS REVIEW! 1. Label the path of electrons through the light reactions of photosynthesis using the illustration below. A. Include PSII and PSI and label all the complexes involved i. Which complex pushes H* across the membrane? ii. Where do these electrons end up? iii. What is the purpose of splitting H2O? iv. Where do the light reactions take place? 2H2D Ot ENR NAOD ADP photolyetemi photosyetemi wlochtone be-...
What is answer of #10?? Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1....
What is answer of #10??
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need only be...
What is answer of #9??? Help me Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis /...
What is answer of #9???
Help me
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need...
Give a detailed mechanism for this reaction and give a separation scheme NUCLEOPHILIC ACYL SUBSTITUTION: Synthesis...
Give a detailed mechanism for this reaction and give a separation
scheme
NUCLEOPHILIC ACYL SUBSTITUTION: Synthesis of an Ester Isoamyl acetate (Banana Oil) Purpose This experiment demonstrat and alcohol. The technique of refluxing the reaction mixture is introduced. es the procedure for the synthesis of an ester from a carboxylic acid Esters are an important functional group in organic chemistry, and esters are found widely distributed in nature. Many lower molecular weight esters are associated with natural fuit flavors and...
Draw the SN1 mechanism of the reaction between (R)-3-methylhexane
and ethanol. Show lone pairs, electron pushing arrows, 3-D view to
reflect appropriate stereochemistry, reactants,intermediates, and
products. name the product. draw and completely label a reaction
energy diagram corresponding to the mechanism you have drawn.
B. Draw the Snl mechanism of the reaction between (R)-3-bromo-3-methylhexane and ethanol. Show lone pairs, electron pushing arrows, 3-D view to reflect appropriate stereochemistry, reactants, intermediates, and products. You do not have to show transition states....
organic chem, i like your answer immediately
3. A compound with molecular formula of C4H8O2 has one singlet H-NMR peak at 8 3.7 ppm. This compound has a strong IR absorption at 1122 cm!. There is no carbonyl group in this compound. What is the structure of this compound? A. B. C D. 3 1
answer all parts
Draw the mechanism (electron pushing and main organic product) for the first step of this Kolbe-Schmitt reaction. The Kolbe-Schmitt reaction adds a carboxyl group ortho to the hydroxyl group of phenol. After acidification, salicylic acid is produced. он 1) NaOH OH 2) CO, (100 atm, 125°C) 3) H0 DO A ¢ % o Ć . I I O Z o os Draw the starting material and electron pushing arrows for the third step of this Kolbe-Schmitt reaction....
2. (a) (i) Draw an arrow-pushing mechanism that illustrates the electron flow in the acid-base reaction below. Use the structures shown below in your arrow-pushing mechanism. (4pts for correct mechanism). (ii) Using pKa values indicated in Table 1.8 (round to nearest whole number) and estimate the equilibrium constant for this reaction (Keq). Show work which led to this value. (3pts for work, 1pt for correct Keq indicated). (iii) Draw a base (assuming the same acid provided below) that would reverse...
I need help with this homework. I've been sick and out of
class and don't know how to do it!! :(
1. Below is a nanodragster...
... wm ve Serected at random for grading, but a full answer key will be posted to Blackboard. 1. Below is a nanodragster. YES, we can make machines-cars, even at the nano-scale, the sizes of molecules. This little nanodragster has some nifty features. Its chassis is rigid like the chassis of a real car....
How to solve alkene and alkyne reactions
- Merdanym i Act antalyzod Hrdian ca Come Lazarmistry I V WORKSHOP #9 Alkenes, Alkynes, Reactions 1. Give a reasonable mechanism for the following reaction. Clearly show intermediates and show the movement of electron pairs with curved arrows. all сна H20. (H2SO4) H₃C CH₂ нас он H3CX сна 2. The addition of HBr to 2-methylpropene can, in principle, give either 1-bromo-2- methylpropane or 2-bromo-2-methylpropane. In reality, only the latter is formed. Show mechanisms...
YOU MUST ANSWER THE FOLLOWING QUESTIONS ON YOUR OWN PRIOR TO CLASS REVIEW! 1. Label the path of electrons through the light reactions of photosynthesis using the illustration below. A. Include PSII and PSI and label all the complexes involved i. Which complex pushes H* across the membrane? ii. Where do these electrons end up? iii. What is the purpose of splitting H2O? iv. Where do the light reactions take place? 2H2D Ot ENR NAOD ADP photolyetemi photosyetemi wlochtone be-...
What is answer of #10??
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need only be...
What is answer of #9???
Help me
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need...
Give a detailed mechanism for this reaction and give a separation
scheme
NUCLEOPHILIC ACYL SUBSTITUTION: Synthesis of an Ester Isoamyl acetate (Banana Oil) Purpose This experiment demonstrat and alcohol. The technique of refluxing the reaction mixture is introduced. es the procedure for the synthesis of an ester from a carboxylic acid Esters are an important functional group in organic chemistry, and esters are found widely distributed in nature. Many lower molecular weight esters are associated with natural fuit flavors and...
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