Organic Chemistry
1. Predict the oxidation product of treating dihydronaphthalene with the reagents shown below. Only draw one enantiomer if more than one is possible. Include H'son chirality centers. (THF = tetrahydrofuran) (ABOVE)
2. Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C5H5NH )(ClCrO3–), commonly known as PCC. Draw theproposed (neutral) intermediate and the organic product in the oxidation of 1-butanol by PCC when carried out in an anhydrous solvent such as CH2Cl2.
Homework Answers
Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C5H5NH )(ClCrO3–),...
Alcohols can be oxidized by
chromic acid derivatives. One such reagent is pyridinium
chlorochromate, (C5H5NH )(ClCrO3–), commonly known as PCC. Draw the
proposed (neutral) intermediate and the organic product in the
oxidation of 1-butanol by PCC when carried out in an anhydrous
solvent such as CH2Cl2.
Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C5H5NH*)(CICro3 commonly known as PCC. Draw the proposed (neutral) intermediate and the organic product in the oxidation of 1-butanol by...
Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C5H5NH )(ClCrO3...
Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C5H5NH )(ClCrO3 Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C5H5NH )(ClCrO3-), commonly known as PCC. Draw the proposed (neutral) intermediate and the organic product in the oxidation of 1-butanol by PCC when carried out in an anhydrous solvent such as CH2Cl2.
Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C5H5NH+)(CICrO3-), commonly...
Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C5H5NH+)(CICrO3-), commonly known as PCC. Draw the proposed (neutral) intermediate and the organic product in the oxidation of 1-butanol by PCC when carried out in an anhydrous solvent such as CH2Cl2. Intermediate Product PCC ЛЛон OH CH,CI,
Predict the oxidation product of treating the given alkene with reagents shown below.
Predict the oxidation product of treating the given alkene with reagents shown below. only draw one enantiomer if more than one is possible. Include H's on chirality centers. (THF=tetrahydrofuran)
Predict the oxidation product of treating dihydronaphthalene with the reagents shown below. Only draw one enantiomer...
Predict the oxidation product of treating dihydronaphthalene with the reagents shown below. Only draw one enantiomer if more than one is possible. Include H's on chirality centers. Assume only one of the double bonds shown will react. Which one will it be? (A stability-reactivity principle will apply.) 4 dihydronaphthalene
Predict the oxidation product of treating dihydronaphthalene with the reagents shown below. Only draw one enantiomer if...
Predict the oxidation product of treating dihydro naphthalene with the reagents shown below. Only draw one enantiomer if more
than one is possible. Include H's on chirality centers. (mCPBA =
meta-chloroperoxybenzoic acid) (1) mCPBA, CH2CL2----------------------->dihydro naphthalene (2) H+, H2O
Predict the oxidation product of treating dihydronaphthalene
Predict the oxidation product of treating dihydronaphthalene with the reagents shown below. Only draw one enantiomer if more than one is possible. Include H's onchirality centers. (mCPBA= meta-chloroperoxybenzoic acid)
Draw the major organic product of the reaction shown below. -OH pyridinium chlorochromate (PCC) CH2Cl2 •...
Draw the major organic product of the reaction shown below. -OH pyridinium chlorochromate (PCC) CH2Cl2 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. ChemDoodle
Alcohols can be oxidized by
chromic acid derivatives. One such reagent is pyridinium
chlorochromate, (C5H5NH )(ClCrO3–), commonly known as PCC. Draw the
proposed (neutral) intermediate and the organic product in the
oxidation of 1-butanol by PCC when carried out in an anhydrous
solvent such as CH2Cl2.
Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C5H5NH*)(CICro3 commonly known as PCC. Draw the proposed (neutral) intermediate and the organic product in the oxidation of 1-butanol by...
Alcohols can be oxidized by chromic acid derivatives. One such reagent is pyridinium chlorochromate, (C5H5NH+)(CICrO3-), commonly known as PCC. Draw the proposed (neutral) intermediate and the organic product in the oxidation of 1-butanol by PCC when carried out in an anhydrous solvent such as CH2Cl2. Intermediate Product PCC ЛЛон OH CH,CI,
Predict the oxidation product of treating dihydronaphthalene with the reagents shown below. Only draw one enantiomer if more than one is possible. Include H's on chirality centers. Assume only one of the double bonds shown will react. Which one will it be? (A stability-reactivity principle will apply.) 4 dihydronaphthalene
Predict the oxidation product of treating dihydro naphthalene with the reagents shown below. Only draw one enantiomer if more
than one is possible. Include H's on chirality centers. (mCPBA =
meta-chloroperoxybenzoic acid) (1) mCPBA, CH2CL2----------------------->dihydro naphthalene (2) H+, H2O
Draw the major organic product of the reaction shown below. -OH pyridinium chlorochromate (PCC) CH2Cl2 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. ChemDoodle
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