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A set of three nucleophilic displacement reactions is shown below: CH3 CI CH2CI CI CH3 H20,...
A set of three nucleophilic displacement reactions is shown below: - Br -Br CH3 Hас CHз...
A set of three nucleophilic displacement reactions is shown below: - Br -Br CH3 Hас CHз В A NaCN CHнон SN2 reaction Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest? C A set of three nucleophilic displacement reactions is shown below: CH3 NaCN SN2 reaction CH3CHCH2CH2-X dimethylformamide (DMF) C, X A, X Br B, X CI Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or...
A set of three nucleophilic displacement reactions is shown below: Which reaction (A, B, or C)...
A set of three nucleophilic displacement reactions is shown
below:
Which reaction (A, B, or C) proceeds the fastest?
Which reaction (A, B, or C) proceeds the slowest?
A set of three nucleophilic displacement reactions is shown below:Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest?
Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed....
Identify the mechanism by which each of the reactions above
proceeds from among the mechanisms listed. Use the letters
a - i for your answers.
Methanol to + + NaOCH3 NOCH Mothands t º + HOCH • NAGI HOCHZ + NaCl OH NaHCO3 o + H2O + CO2 + Nal a = Proton transfer b = Lewis acid base c = Radical chain substitution d=Radical chain addition e = Electrophilic addition f=E1 Elimination g=E2 Elimination h=Syl Nucleophilic substitution i= Sy2...
Draw the major organic product(s) of the following reaction. CH3 HỌC-C CI CH3 + NaOH 2rea...
Draw the major organic product(s) of the following reaction. CH3 HỌC-C CI CH3 + NaOH 2rea • You do not have to consider stereochemistry. • If no reaction occurs, draw the organic starting material. • When Sn1 & El pathways compete, show both the substitution and the elimination products. Separate multiple products using the + sign from the drop-down menu. Do not include counter-ions, e.g., Na", 1", in your answer. Draw the major organic product(s) of the following reaction. HEC-Br...
H Ph CI + NaOH n ogle - listen NO2 a = Proton transfer d =...
H Ph CI + NaOH n ogle - listen NO2 a = Proton transfer d = Electrophilic addition g=Syl Nucleophilic substitution h = Sy2 Nucleophilic substitution b = Lewis acid base e=E1 Elimination c=Radical chain substitution f=E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 1. Submit Answer Retry Entire Group 3 more group attempts remaining
[Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl...
[Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. CH2CH3 CH3CH2CH2CCH2CH3 Submit Answer Retry Entire Group 9 more group attempts remaining The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Br NaOCCH, . CH3CH2CHCH 1. none h. HBr 1.H20 e. "CCH3 f. Br j. Nat 9. HOCCH3 k. "OCCH3 Which letter designates the electrophilic carbon at which substitution occurs? (If no...
What is the relationship between each pair of molecules shown below? CH3 CH3 CH3 Submit Answer...
What is the relationship between each pair of molecules shown below? CH3 CH3 CH3 Submit Answer Retry Entire Group 9 more group attempts remaining
1. 2. NO2 1. CI NO2 2· OH O Na +Na NH2 +NH3 a -Proton transfer...
1.
2.
NO2 1. CI NO2 2· OH O Na +Na NH2 +NH3 a -Proton transfer b Lewis acid base c = Radical chain substitution d-Radical chain addition e - Electrophilic addition f El Elimination gE2 Elimination -Syl Nucleophilic substitution Sy2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. Submit Answer Retry Entire Group 8 more group attempts remaining
O H2N-OH 2. нса a Electrophilic addition b-E2 Elimination d- Sy2 Nucleophilic substitution-Nucleophilic subs at carbonyl(acyl...
O H2N-OH 2. нса a Electrophilic addition b-E2 Elimination d- Sy2 Nucleophilic substitution-Nucleophilic subs at carbonyl(acyl Xfer) e-Electrophilic aromatic substitution h -Conjugate (nucleophilic) addn SNI Nucleophilic substitution r-Carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 2. Submit Answor Retry Entire Group 9 more group attempts remaining
1 Br NaBr NaOH HO сHз CH3 Нс — она 2. Hао Нассн, CH3 a Proton transfer Radical chain addition d g E2 Elimination h SNl...
1 Br NaBr NaOH HO сHз CH3 Нс — она 2. Hао Нассн, CH3 a Proton transfer Radical chain addition d g E2 Elimination h SNl Nucleophilic substitution b Lewis acid/base e Electrophilic addition i S2 Nucleophilic substitution c Radical chain substitution f= E1 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers 1. 2 Submit Answer Retry Entire Group 8 more group...
A set of three nucleophilic displacement reactions is shown below: - Br -Br CH3 Hас CHз В A NaCN CHнон SN2 reaction Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest? C A set of three nucleophilic displacement reactions is shown below: CH3 NaCN SN2 reaction CH3CHCH2CH2-X dimethylformamide (DMF) C, X A, X Br B, X CI Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or...
A set of three nucleophilic displacement reactions is shown
below:
Which reaction (A, B, or C) proceeds the fastest?
Which reaction (A, B, or C) proceeds the slowest?
A set of three nucleophilic displacement reactions is shown below:Which reaction (A, B, or C) proceeds the fastest? Which reaction (A, B, or C) proceeds the slowest?
Identify the mechanism by which each of the reactions above
proceeds from among the mechanisms listed. Use the letters
a - i for your answers.
Methanol to + + NaOCH3 NOCH Mothands t º + HOCH • NAGI HOCHZ + NaCl OH NaHCO3 o + H2O + CO2 + Nal a = Proton transfer b = Lewis acid base c = Radical chain substitution d=Radical chain addition e = Electrophilic addition f=E1 Elimination g=E2 Elimination h=Syl Nucleophilic substitution i= Sy2...
Draw the major organic product(s) of the following reaction. CH3 HỌC-C CI CH3 + NaOH 2rea • You do not have to consider stereochemistry. • If no reaction occurs, draw the organic starting material. • When Sn1 & El pathways compete, show both the substitution and the elimination products. Separate multiple products using the + sign from the drop-down menu. Do not include counter-ions, e.g., Na", 1", in your answer. Draw the major organic product(s) of the following reaction. HEC-Br...
H Ph CI + NaOH n ogle - listen NO2 a = Proton transfer d = Electrophilic addition g=Syl Nucleophilic substitution h = Sy2 Nucleophilic substitution b = Lewis acid base e=E1 Elimination c=Radical chain substitution f=E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 1. Submit Answer Retry Entire Group 3 more group attempts remaining
[Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. CH2CH3 CH3CH2CH2CCH2CH3 Submit Answer Retry Entire Group 9 more group attempts remaining The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Br NaOCCH, . CH3CH2CHCH 1. none h. HBr 1.H20 e. "CCH3 f. Br j. Nat 9. HOCCH3 k. "OCCH3 Which letter designates the electrophilic carbon at which substitution occurs? (If no...
What is the relationship between each pair of molecules shown below? CH3 CH3 CH3 Submit Answer Retry Entire Group 9 more group attempts remaining
1.
2.
NO2 1. CI NO2 2· OH O Na +Na NH2 +NH3 a -Proton transfer b Lewis acid base c = Radical chain substitution d-Radical chain addition e - Electrophilic addition f El Elimination gE2 Elimination -Syl Nucleophilic substitution Sy2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. Submit Answer Retry Entire Group 8 more group attempts remaining
O H2N-OH 2. нса a Electrophilic addition b-E2 Elimination d- Sy2 Nucleophilic substitution-Nucleophilic subs at carbonyl(acyl Xfer) e-Electrophilic aromatic substitution h -Conjugate (nucleophilic) addn SNI Nucleophilic substitution r-Carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 2. Submit Answor Retry Entire Group 9 more group attempts remaining
1 Br NaBr NaOH HO сHз CH3 Нс — она 2. Hао Нассн, CH3 a Proton transfer Radical chain addition d g E2 Elimination h SNl Nucleophilic substitution b Lewis acid/base e Electrophilic addition i S2 Nucleophilic substitution c Radical chain substitution f= E1 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers 1. 2 Submit Answer Retry Entire Group 8 more group...
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