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please provide mechanism, specifically the first intermediate
portion
KNH2 NO2 NH3 (liquid) -38 °C MT2 Mastery...
CICI CH3CH2OH 25 °C MT2 Mastery 1 Predict the Product HCI (catalytic) om ". i THF/H20...
CICI CH3CH2OH 25 °C MT2 Mastery 1 Predict the Product HCI (catalytic) om ". i THF/H20 65 °C MT2 Mastery 5 Provide the structure of the charged intermediate from the second step of the mechanism that leads to these products? HN KNH2 NO2 NO2 NH3 (liquid) -38 °C MT2 Mastery 6 Provide the structure of first intermediate of the mechanism that leads to this products?
provide the structure of the first intermediate of the mechanism that leads to the product above...
provide the structure of the first intermediate of the mechanism
that leads to the product above
X 0 Spectroscopy Unknown Pre-tect x G 1-hydroxybutan-2-one Google + C o app.tophat.com/e/170799/assigned reanic Chemistoclecture with MMD (SD201 MT2 Mastery 4 - Image HCI (catalytic) CH3CH2OH mol. sieves 78 °C MT2 Mastery 4 Provide the structure of first intermediate of the mechanism that leads to this products? Type here to search
The liquid portion of a diet is to provide at least 300 calories, 36 units of...
The liquid portion of a diet is to provide at least 300 calories, 36 units of vitamin A, and 90 units of vitamin C daily. A cup of one dietary drink provides 60 calories, 12 units of vitamin A, and 10 units of vitamin C. A cup of another dietary drink provides 60 calories, 6 units of vitamin A, and 30 units of vitamin C. Suppose that the first dietary drink costs $0.12 per cup while the second dietary drink...
I am not sure what I did wrong. I believe the answer to the first portion...
I am not sure what I did wrong. I believe the answer to the
first portion is correct, but I am not sure how to approach the
second. Please be very clear in drawing the mechanism and final
product. Please clearly circle the answers.
D CHANH dana -CH2NH-CCH2- o H2O H2SO4 Hoo a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown • You do not have to consider stereochemistry. • Do not include counter-ions, e.g., Na",...
Please provide the mechanism for steps1 through 4 including any relevant resonance structures. STEP 1 NH2...
Please provide the mechanism for steps1 through 4
including any relevant resonance structures.
STEP 1 NH2 STEP 2 liquid NH3 33 °C, 5 hrs Cl NH2 O Cl Cl NaOH (1 eq.), 10 °C, 30 mins, with dioxane as solvent Cl Cl Cl pyridine (solvent), heat at STEP 3 reflux with Dean-Stark Trap, 1 hour H3C но STEP 4 1. NaOCH3 in CH3OH 2. CHal in DMF, 30 min Cl Cl Diazepam (Valium) NOTE the 7-membered ring!!
1. Provide the products of the reaction below and a detailed reaction mechanism using curved arrows...
1. Provide the products of the reaction below and a detailed reaction mechanism using curved arrows to indicate the movement of electrons. (a) (b) КОН (c) Note that formation of 4- or 7-membered rings is disfavored. Hiyo KOH acidie workup 2. An interesting problem that involves a bit of review (imines and Grignard chemistry) and application of what you previously learned to a new reaction: The Carbon of an imine functional group (i.e. R.C-NR) is sufficiently electron deficient to be...
Please show detailed arrow-pushing mechanism. Best regards. C) Please provide the product of the following reaction...
Please show detailed arrow-pushing
mechanism.
Best regards.
C) Please provide the product of the following reaction and concisely explain why you get the observed constitutional isomer. Drawing the appropriate orbitals will really help to explain your answer. (2 points box, 4 points explanation, 6 points total section). 1 H O-Na H Mel
please answer all parts, thanks! 1. More substituted alkenes are more stable than less substituted alkenes....
please answer all parts, thanks!
1. More substituted alkenes are more stable than less substituted alkenes. Show the orbital overlap that helps to explain this observation. 2. Why is the heat of hydrogenation for an alkene exothermic? Analyze the bonds that are changing. AH = -30 kcal/mol Explain: + H2 3. Treating alkene "A" below with HBr can lead to a number of products. "A" SM + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters...
please show a detailed mechanism from X-Y, X-Z, Z-W. 2. Compound X, with chemical formula C...
please show a detailed mechanism from X-Y, X-Z, Z-W.
2. Compound X, with chemical formula C Ho, gives 1,3-dimethylcyclopentane when treated with Hz Over Pt. That same compound, when treated with hot and concentrated KMnO, produces carbon dioxide and Y. Compound X reacts with two equivalents of HBr in the presence of a peroxyether to form compound Z, with chemical formula C H2Br2. When pound Z is heated in methanol it yields compound W, among others. (a) (6 pts., 3...
I only need help with 5D) , please explain the thinking behind the rationale 5. Consider...
I only need help with 5D) , please explain the thinking
behind the rationale
5. Consider the reaction shown below: H CH3 Brg/ CH2Cl2 C=C meso-2,3-dibromobutane (as the sole product) Hac H a) Provide below a step-by-step mechanism for that reaction (10 points) When the reaction above is carried out with 1-phenyl-1-propene, four products are formed: | H Ph C=Ć Brz/ CH2Cl2 Br. Br BECOMH (19%) HU HECH Br Ph ul.C-CAH 181%] and нус Br (+ enantiomer) Hac Pn (+...
CICI CH3CH2OH 25 °C MT2 Mastery 1 Predict the Product HCI (catalytic) om ". i THF/H20 65 °C MT2 Mastery 5 Provide the structure of the charged intermediate from the second step of the mechanism that leads to these products? HN KNH2 NO2 NO2 NH3 (liquid) -38 °C MT2 Mastery 6 Provide the structure of first intermediate of the mechanism that leads to this products?
provide the structure of the first intermediate of the mechanism
that leads to the product above
X 0 Spectroscopy Unknown Pre-tect x G 1-hydroxybutan-2-one Google + C o app.tophat.com/e/170799/assigned reanic Chemistoclecture with MMD (SD201 MT2 Mastery 4 - Image HCI (catalytic) CH3CH2OH mol. sieves 78 °C MT2 Mastery 4 Provide the structure of first intermediate of the mechanism that leads to this products? Type here to search
I am not sure what I did wrong. I believe the answer to the
first portion is correct, but I am not sure how to approach the
second. Please be very clear in drawing the mechanism and final
product. Please clearly circle the answers.
D CHANH dana -CH2NH-CCH2- o H2O H2SO4 Hoo a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown • You do not have to consider stereochemistry. • Do not include counter-ions, e.g., Na",...
Please provide the mechanism for steps1 through 4
including any relevant resonance structures.
STEP 1 NH2 STEP 2 liquid NH3 33 °C, 5 hrs Cl NH2 O Cl Cl NaOH (1 eq.), 10 °C, 30 mins, with dioxane as solvent Cl Cl Cl pyridine (solvent), heat at STEP 3 reflux with Dean-Stark Trap, 1 hour H3C но STEP 4 1. NaOCH3 in CH3OH 2. CHal in DMF, 30 min Cl Cl Diazepam (Valium) NOTE the 7-membered ring!!
1. Provide the products of the reaction below and a detailed reaction mechanism using curved arrows to indicate the movement of electrons. (a) (b) КОН (c) Note that formation of 4- or 7-membered rings is disfavored. Hiyo KOH acidie workup 2. An interesting problem that involves a bit of review (imines and Grignard chemistry) and application of what you previously learned to a new reaction: The Carbon of an imine functional group (i.e. R.C-NR) is sufficiently electron deficient to be...
Please show detailed arrow-pushing
mechanism.
Best regards.
C) Please provide the product of the following reaction and concisely explain why you get the observed constitutional isomer. Drawing the appropriate orbitals will really help to explain your answer. (2 points box, 4 points explanation, 6 points total section). 1 H O-Na H Mel
please answer all parts, thanks!
1. More substituted alkenes are more stable than less substituted alkenes. Show the orbital overlap that helps to explain this observation. 2. Why is the heat of hydrogenation for an alkene exothermic? Analyze the bonds that are changing. AH = -30 kcal/mol Explain: + H2 3. Treating alkene "A" below with HBr can lead to a number of products. "A" SM + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters...
please show a detailed mechanism from X-Y, X-Z, Z-W.
2. Compound X, with chemical formula C Ho, gives 1,3-dimethylcyclopentane when treated with Hz Over Pt. That same compound, when treated with hot and concentrated KMnO, produces carbon dioxide and Y. Compound X reacts with two equivalents of HBr in the presence of a peroxyether to form compound Z, with chemical formula C H2Br2. When pound Z is heated in methanol it yields compound W, among others. (a) (6 pts., 3...
I only need help with 5D) , please explain the thinking
behind the rationale
5. Consider the reaction shown below: H CH3 Brg/ CH2Cl2 C=C meso-2,3-dibromobutane (as the sole product) Hac H a) Provide below a step-by-step mechanism for that reaction (10 points) When the reaction above is carried out with 1-phenyl-1-propene, four products are formed: | H Ph C=Ć Brz/ CH2Cl2 Br. Br BECOMH (19%) HU HECH Br Ph ul.C-CAH 181%] and нус Br (+ enantiomer) Hac Pn (+...
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