What is the mechanism for the L-phenylalanine using sodium nitrate under acid conditions as H2SO4 (...
What is the mechanism for the L-phenylalanine using sodium nitrate under acid conditions as H2SO4 ( two Sn2 reactions)? Show arrows and explain.
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What is the mechanism for the L-phenylalanine using sodium
nitrate under acid conditions as H2SO4 (...
Sodium hydroxide is added to a 0.1 M solution of phenylalanine. Phenylalanine is a diprotic acid...
Sodium hydroxide is added to a 0.1 M solution of phenylalanine. Phenylalanine is a diprotic acid with two pKas, 2.20 for the carboxylic acid group and 9.31 for the ammonium functional group. When the pH 5.93, the principal species is 10.10 , the principal species is and when the pH a. H2L*; H2L b. HL; L c. H2L*; L d. H2L; HL e. HL; HL
Hydration of alkenes under aqueous acidic conditions. Draw the detailed stepwise mechanism for this reaction. Be...
Hydration of alkenes under aqueous acidic conditions. Draw the detailed stepwise mechanism for this reaction. Be sure to show all steps, intermediates, formal charges, and show the movement of electrons with curved arrows. You do not need to draw transition states. H2SO4 H20 ?? The hydration of alkynes can also occur under aqueous acidic conditions however, instead of forming the alcohol, a ketone is formed. Draw the detailed stepwise mechanism for the conversion of the alkyne to the ketone (one...
AI(NO3)3(aq) + Na3PO4(aq) → E. Neutralization Reactions 1. nitric acid(aq) + sodium hydroxide(aq) sodium nitrate(aq) +...
AI(NO3)3(aq) + Na3PO4(aq) → E. Neutralization Reactions 1. nitric acid(aq) + sodium hydroxide(aq) sodium nitrate(aq) + water(1) HNO3(aq) + NaOH(aq) → 2. sulfuric acid(aq) + sodium hydroxide(aq) → sodium sulfate(aq) + water(1) H2SO4(aq) + NaOH(aq) → sodium phosphate(aq) + water(1) 3. phosphoric acid(aq) + sodium hydroxide(aq) H3PO4(aq) + NaOH(aq)
Sodium Nitrate + Sulfuric Acid Observation no real change Nanoa laa) + H2SO4 lac) + HNOzlaq)...
Sodium Nitrate + Sulfuric Acid Observation no real change Nanoa laa) + H2SO4 lac) + HNOzlaq) Naas Molecular Equation Complete Ionic Equation Net Ionic Equation Driving Force . Nickel(II) Chloride + Copper(II) Sulfate Observation changed to a green nue Molecular Equation Complete Ionic Equation Net Ionic Equation Driving Force ... ... . .. . .
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and...
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. mer 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3C CI CH OH CH2CH3 општироотип солио 3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms NaCN...
1. Under second-order conditions (strong base/nucleophile), SN2 and E2 reactions may occur simultaneously and compete with...
1. Under second-order conditions (strong base/nucleophile),
SN2 and E2 reactions may occur simultaneously and
compete with each other.
Show what products might be expected from the reaction of
2-bromo-3-methylbutane (a moderately hindered 2∘ alkyl halide) with
sodium ethoxide.
2.Under second-order conditions (strong base/nucleophile),
SN2 and E2 reactions may occur simultaneously and
compete with each other.
Show what products might be expected from the reaction of
2-bromo-3-methylbutane (a moderately hindered 2∘ alkyl halide) with
sodium ethoxide
3.. Provide the structure of...
The following reaction takes place in acidic conditions under rigorous heating. Complete the reaction mechanism adding...
The following reaction takes place in acidic conditions under
rigorous heating. Complete the reaction mechanism adding missing
atoms and using lone pairs, charges, and curved arrows as
necessary. Ignore hydrogen sulfate in boxes 2 and 3.
The following reaction takes place in acidic conditions under rigorous heating. Complete the reaction mechanism adding missing atoms and using lone pairs, charges, and curved arrows as necessary. Ignore hydrogen sulfate in boxes 2 and 3
1.) What is the order of reactivity of the following reagents under SN1 conditions? Under SN2...
1.) What is the order of reactivity of the following reagents under SN1 conditions? Under SN2 conditions? Draw the structures of each using the bond line method and explain your answers. 1-methyl-1-bromocyclohexane, 1-bromopropane, 2-bromohexane 2.) What is the order of reactivity of the following reagents under SN1 conditions? Under SN2 conditions? Explain your answers. CH3CH=CHBr, CH3CH=CHCH2Br, CH3CH2CH2Br 3.) We did not use crotyl chloride in this experiment. However, based on your knowledge of SN1 and SN2 predict the behavior of...
show a mechanism of formatiin if the following enol under base catalyzed conditions We were unable...
show a mechanism of formatiin if the following enol under base
catalyzed conditions
We were unable to transcribe this imageShow a mechanism of formation of the following enol under base-catalyzed conditions: For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do n use abbreviations such as Me or Ph. Step 1 0 Get help answering Molecular Drawing question Draw step 1 of...
Needing help with this ASAP, thanks! 2. The nitrate under neutral conditions. This may be seen...
Needing help with this ASAP, thanks!
2. The nitrate under neutral conditions. This may be seen by applying Le Chatelier's Principle. Write the balanced half-rxn happen if the rxn conditions were changed from acidic to neutral. ion is an oxidizing agent. However, it is a much stronger OA under acidic conditions than ction of the nitrate ion to nitrogen monoxide under acidic conditions, and explain what will
Sodium hydroxide is added to a 0.1 M solution of phenylalanine. Phenylalanine is a diprotic acid with two pKas, 2.20 for the carboxylic acid group and 9.31 for the ammonium functional group. When the pH 5.93, the principal species is 10.10 , the principal species is and when the pH a. H2L*; H2L b. HL; L c. H2L*; L d. H2L; HL e. HL; HL
Hydration of alkenes under aqueous acidic conditions. Draw the detailed stepwise mechanism for this reaction. Be sure to show all steps, intermediates, formal charges, and show the movement of electrons with curved arrows. You do not need to draw transition states. H2SO4 H20 ?? The hydration of alkynes can also occur under aqueous acidic conditions however, instead of forming the alcohol, a ketone is formed. Draw the detailed stepwise mechanism for the conversion of the alkyne to the ketone (one...
AI(NO3)3(aq) + Na3PO4(aq) → E. Neutralization Reactions 1. nitric acid(aq) + sodium hydroxide(aq) sodium nitrate(aq) + water(1) HNO3(aq) + NaOH(aq) → 2. sulfuric acid(aq) + sodium hydroxide(aq) → sodium sulfate(aq) + water(1) H2SO4(aq) + NaOH(aq) → sodium phosphate(aq) + water(1) 3. phosphoric acid(aq) + sodium hydroxide(aq) H3PO4(aq) + NaOH(aq)
Sodium Nitrate + Sulfuric Acid Observation no real change Nanoa laa) + H2SO4 lac) + HNOzlaq) Naas Molecular Equation Complete Ionic Equation Net Ionic Equation Driving Force . Nickel(II) Chloride + Copper(II) Sulfate Observation changed to a green nue Molecular Equation Complete Ionic Equation Net Ionic Equation Driving Force ... ... . .. . .
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. mer 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3C CI CH OH CH2CH3 општироотип солио 3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms NaCN...
1. Under second-order conditions (strong base/nucleophile),
SN2 and E2 reactions may occur simultaneously and
compete with each other.
Show what products might be expected from the reaction of
2-bromo-3-methylbutane (a moderately hindered 2∘ alkyl halide) with
sodium ethoxide.
2.Under second-order conditions (strong base/nucleophile),
SN2 and E2 reactions may occur simultaneously and
compete with each other.
Show what products might be expected from the reaction of
2-bromo-3-methylbutane (a moderately hindered 2∘ alkyl halide) with
sodium ethoxide
3.. Provide the structure of...
The following reaction takes place in acidic conditions under
rigorous heating. Complete the reaction mechanism adding missing
atoms and using lone pairs, charges, and curved arrows as
necessary. Ignore hydrogen sulfate in boxes 2 and 3.
The following reaction takes place in acidic conditions under rigorous heating. Complete the reaction mechanism adding missing atoms and using lone pairs, charges, and curved arrows as necessary. Ignore hydrogen sulfate in boxes 2 and 3
show a mechanism of formatiin if the following enol under base
catalyzed conditions
We were unable to transcribe this imageShow a mechanism of formation of the following enol under base-catalyzed conditions: For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do n use abbreviations such as Me or Ph. Step 1 0 Get help answering Molecular Drawing question Draw step 1 of...
Needing help with this ASAP, thanks!
2. The nitrate under neutral conditions. This may be seen by applying Le Chatelier's Principle. Write the balanced half-rxn happen if the rxn conditions were changed from acidic to neutral. ion is an oxidizing agent. However, it is a much stronger OA under acidic conditions than ction of the nitrate ion to nitrogen monoxide under acidic conditions, and explain what will
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