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Right answer pls,for right one
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Predict the organic product for the following reaction...
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...
Predict the major organic product of the following reaction and complete its mechanism below. 1) NaOEt/EtOH...
Predict the major organic product of the following reaction and complete its mechanism below. 1) NaOEt/EtOH 2) CH3CH2CH2Br 3) dilute NaOH/heat 4) H30* 5) heat Complete the curved-arrow mechanism for the scheme below by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows. :O O: :Br. CH3CH2OH Do not show curved arrows for this step. Added acid Dilute HH NaOH and heat hydrolyzes the ester. O: Na Br - H20, Na* O: 100-150 °C O:
Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when...
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 conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. Select the option that describes the mechanism of the reaction above. S_N1 S_N2 E1 E2
Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when...
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 conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. Select the option that describes the mechanism of the reaction above. S_N1 S_N2 E1 E2
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. Use curved arrows to show the conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. CH3 :Ci: CH3CH2OH -Cl b) Select the option that describes the mechanism of the reaction above. O E1 O E2
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. Use curved arrows to show the conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. CH3 :ci: СНЫСн,он HO b) Select the option that describes the mechanism of the reaction above. 10 SNI OSN2 Ο Ε1 lo ez
please do the mexhanism Predict the organic product for the following reaction and complete the arrow...
please do the mexhanism
Predict the organic product for the following reaction and complete the arrow pushing mechanism. НСІ Complete the mechanism for the reaction by adding the missing curved arrows, atoms, bonds, charges, and nonbonding electron pairs. Note the resonance arrow(s) in the scheme. C: H 1L H H 1L -H a: 0 H Introduced a second protonated aldehyde molecule in the panel on the left. 11 The ungraded panel below has two steps summarized into one. ö: 'H...
Predict the organic products of the following Grignard reaction. Ma 1) CH3MgCl (excess) Et20 2) H30...
Predict the organic products of the following Grignard reaction. Ma 1) CH3MgCl (excess) Et20 2) H30 Complete the mechanism for the above reaction below. Add any missing curved arrows, bonds, atoms nonbonding electron pairs, and charges
a) Predict the organic product of the reaction of 2-methylpropan-1-ol with phosphorus tribromide. b) Phosphorus tribro...
a) Predict the organic product of the reaction of
2-methylpropan-1-ol with phosphorus tribromide.
b) Phosphorus tribromide makes the oxygen of the alcohol a good
leaving group and also provides the nucleophilic bromide. Complete
the last step of the mechanism below by using curved arrows.
a) predict the organic product of the reaction of 2-methylpropan-1-ol with phosphorus tribromide. B) Phosphorus tribomide...
a) predict the organic product of the reaction of
2-methylpropan-1-ol with phosphorus tribromide. B) Phosphorus
tribomide makes the oxygen of the alcohol a good leaving group and
also provides the nucleophilic bromide. Complete the last step of
the mechanism below by using curved arrows.
chl ャ p-Br, : Gr:
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...
Predict the major organic product of the following reaction and complete its mechanism below. 1) NaOEt/EtOH 2) CH3CH2CH2Br 3) dilute NaOH/heat 4) H30* 5) heat Complete the curved-arrow mechanism for the scheme below by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows. :O O: :Br. CH3CH2OH Do not show curved arrows for this step. Added acid Dilute HH NaOH and heat hydrolyzes the ester. O: Na Br - H20, Na* O: 100-150 °C O:
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 conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. Select the option that describes the mechanism of the reaction above. S_N1 S_N2 E1 E2
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 conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. Select the option that describes the mechanism of the reaction above. S_N1 S_N2 E1 E2
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 conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. CH3 :Ci: CH3CH2OH -Cl b) Select the option that describes the mechanism of the reaction above. O E1 O E2
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 conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. CH3 :ci: СНЫСн,он HO b) Select the option that describes the mechanism of the reaction above. 10 SNI OSN2 Ο Ε1 lo ez
please do the mexhanism
Predict the organic product for the following reaction and complete the arrow pushing mechanism. НСІ Complete the mechanism for the reaction by adding the missing curved arrows, atoms, bonds, charges, and nonbonding electron pairs. Note the resonance arrow(s) in the scheme. C: H 1L H H 1L -H a: 0 H Introduced a second protonated aldehyde molecule in the panel on the left. 11 The ungraded panel below has two steps summarized into one. ö: 'H...
Predict the organic products of the following Grignard reaction. Ma 1) CH3MgCl (excess) Et20 2) H30 Complete the mechanism for the above reaction below. Add any missing curved arrows, bonds, atoms nonbonding electron pairs, and charges
a) Predict the organic product of the reaction of
2-methylpropan-1-ol with phosphorus tribromide.
b) Phosphorus tribromide makes the oxygen of the alcohol a good
leaving group and also provides the nucleophilic bromide. Complete
the last step of the mechanism below by using curved arrows.
a) predict the organic product of the reaction of
2-methylpropan-1-ol with phosphorus tribromide. B) Phosphorus
tribomide makes the oxygen of the alcohol a good leaving group and
also provides the nucleophilic bromide. Complete the last step of
the mechanism below by using curved arrows.
chl ャ p-Br, : Gr:
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