1)Predict the product + draw the mechanism
2) Use Frost's circle
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1)Predict the product + draw the mechanism
2) Use Frost's circle
1) Predict the product(s) and...
1) Predict the product(s) and draw the mechanism for when the compound below are treated with...
1) Predict the product(s) and draw the mechanism for when the compound below are treated with chloroethane and AICI3. (1.5 points) 2) Use Frost's circle to construct orbital energy diagram for cyclopentadienyl anion. Clearly draw the orbital energies diagram with the correct the number of electron in each level, label it as aromatic or antiaromatic according to Huckel's rule." (1.5 points) OH
Predict the product(s) and draw the mechanism for when the compound below are treated with excess...
Predict the product(s) and draw the mechanism for when the
compound below are treated with excess chloroethane and
AlCl3.
please help!!!! with distributed a orbitals. IL A 0 0 0 0 0 0 2) Draw...
please help!!!!
with distributed a orbitals. IL A 0 0 0 0 0 0 2) Draw the MOLECULAR ORBITAL (MO) energy diagram for the cyclopentadiene radical and classify the ion as aromatic or antiaromatic. Explain why without using Huckel's rule but rather your MO energy diagram. Use the Polygon method to draw the Molecular Orbital diagram. (6pts)
Draw the molecular orbital diagram using the polygon method of cycloheptatriene anion. Label all the orbitals...
Draw the molecular orbital diagram using the polygon method of cycloheptatriene anion. Label all the orbitals and fill in the electrons in the system. Use the molecular orbital diagram to predict whether the system is non, anti, or aromatic and explain your answer without using huckels rule.
6. Draw both the 1,2- and the 1,4-addition products of the following substrate. Circle the kinetic...
6. Draw both the 1,2- and the 1,4-addition products of the following substrate. Circle the kinetic product (2 pts.). HBE (1 ) 7. Construct an inscribed polygon in the circle provided to illustrate the molecular orbitals for the cycloheptatrienyl anion. Illustrate the relative energies of all the molecular orbitals, label bonding and anti-bonding and assuming this species is planar, assess whether it is non-aromatic, aromatic, or anti-aromatic. Explain why (2 pts.).
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp? hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) Dec 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) 3. Rank the reactivity of the compounds...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) Antanan ENon ordre Energy Bunding aromatic antiaromatic 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) nonovomatic...
2. For the reaction below: a. Predict the most stable product(s) and draw the mechanism Br...
2. For the reaction below: a. Predict the most stable product(s) and draw the mechanism Br OK b. Redraw the product/s) below and label all the non-equivalent carbons. How many sonals would you expect to see in the C NMR of the product? Predict the chemical shifts of each carbon below. c. Redraw the product(s) below and label all the non-equivalent hydrogens. How many signals would you expect to see in the 'H NMR of the product? Predict the chemical...
a) complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction...
a) complete the curved arrow electron-pushing mechanism and
predict the major organic product of the reaction when
1-chloropentane is treated with hydroxide in ethanol as shown
below.
a) Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the Draw the structure of the organic product formed in the reaction. Draw lone pairs. conversion to the product. CH3CH2OH -CI...
Draw a full mechanism for the following transformation and predict the product. Show all the elementary...
Draw a full mechanism for the following transformation and
predict the product. Show all the elementary step(s) being sure to
include all arrows, important electron pairs and any formal charges
if needed.
SHORT ANSWER # 27: Draw a full mechanism for the following transformation and predict the product. Show all the elementary step(s) being sure to include all arrows, important electron pairs and any formal charges if needed. (8 points) H H+ HO hemiacetal product
1) Predict the product(s) and draw the mechanism for when the compound below are treated with chloroethane and AICI3. (1.5 points) 2) Use Frost's circle to construct orbital energy diagram for cyclopentadienyl anion. Clearly draw the orbital energies diagram with the correct the number of electron in each level, label it as aromatic or antiaromatic according to Huckel's rule." (1.5 points) OH
Predict the product(s) and draw the mechanism for when the
compound below are treated with excess chloroethane and
AlCl3.
please help!!!!
with distributed a orbitals. IL A 0 0 0 0 0 0 2) Draw the MOLECULAR ORBITAL (MO) energy diagram for the cyclopentadiene radical and classify the ion as aromatic or antiaromatic. Explain why without using Huckel's rule but rather your MO energy diagram. Use the Polygon method to draw the Molecular Orbital diagram. (6pts)
6. Draw both the 1,2- and the 1,4-addition products of the following substrate. Circle the kinetic product (2 pts.). HBE (1 ) 7. Construct an inscribed polygon in the circle provided to illustrate the molecular orbitals for the cycloheptatrienyl anion. Illustrate the relative energies of all the molecular orbitals, label bonding and anti-bonding and assuming this species is planar, assess whether it is non-aromatic, aromatic, or anti-aromatic. Explain why (2 pts.).
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp? hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) Dec 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) 3. Rank the reactivity of the compounds...
1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) Antanan ENon ordre Energy Bunding aromatic antiaromatic 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) nonovomatic...
2. For the reaction below: a. Predict the most stable product(s) and draw the mechanism Br OK b. Redraw the product/s) below and label all the non-equivalent carbons. How many sonals would you expect to see in the C NMR of the product? Predict the chemical shifts of each carbon below. c. Redraw the product(s) below and label all the non-equivalent hydrogens. How many signals would you expect to see in the 'H NMR of the product? Predict the chemical...
a) complete the curved arrow electron-pushing mechanism and
predict the major organic product of the reaction when
1-chloropentane is treated with hydroxide in ethanol as shown
below.
a) Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the Draw the structure of the organic product formed in the reaction. Draw lone pairs. conversion to the product. CH3CH2OH -CI...
Draw a full mechanism for the following transformation and
predict the product. Show all the elementary step(s) being sure to
include all arrows, important electron pairs and any formal charges
if needed.
SHORT ANSWER # 27: Draw a full mechanism for the following transformation and predict the product. Show all the elementary step(s) being sure to include all arrows, important electron pairs and any formal charges if needed. (8 points) H H+ HO hemiacetal product
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