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The two reactants shown below are combined to bring about a nucleophilic substitution reaction. CH3 +...
The two reactants shown below are combined to bring about a nucleophilic substitution reaction. CH3 + H2O Otos i. H30+ e. "OTos f. OH g. H2O h. "OS j. CH3OH k. none Which letter designates the electrophilic carbon at which substitution occurs? (If no reaction occurs enter the letter corresponding to "none.") Which letter corresponds to the leaving group? 1:1 1 .deicotill 1:1.00 Which letter corresponds to the leaving group? O Which letter designates the nucleophile?
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...
The two reactants shown below are combined to bring about a nucleophilic substitution reaction. F +...
The two reactants shown below are combined to bring about a nucleophilic substitution reaction. F + Nal IT g. HI h. Nat i. none f. HF Which letter designates the electrophilic carbon at which substitution occurs? (If no reaction occurs enter the letter corresponding to "none.") Which letter corresponds to the leaving group? Which letter designates the nucleophile? Submit Answer Try Another Version 1 item attempt remaining
The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Which letter...
The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Which letter designates the electrophilic carbon at which substitution occurs? (If no reaction occurs enter the letter corresponding to "none.") Which letter corresponds to the leaving group? Which letter designates the nucleophile?
[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...
1) State which of the electrophiles given below will react preferentially by i) SN1, ii) by...
1) State which of the electrophiles given below will react
preferentially by i) SN1, ii) by SN2, or iii) capable of reacting
by either of the two mechanisms depending on the given conditions.
How can you affect those conditions to favour SN1 or SN2? Reason
your predictions based on the structures of the compounds. Br-CH3,
Br-CH2CH3, Br-CH(CH3)2, Br-C(CH3)3, Br-CH2-C5H6; C5H6 = phenyl
Introduction Alkyl halides can be prepared from alcohols by reactions with hydrogen halides (HCI, HBr, or HI) via...
Question 20 15 pts OH A) HBr K) Cl2, hv B) NaOH, H2O L) SOCI2 C)...
Question 20 15 pts OH A) HBr K) Cl2, hv B) NaOH, H2O L) SOCI2 C) CH3COONa, DMF M) LiAIH4, THE D) CH3CH2CH2CH2MgBr, ether N) NaBH4, CH3CH2OH E) CH3CH2MgBr, ether O) CH3CH2OH, H2SO4 F) CH3CH2Li, ether P) CH3CH2ONa, CH2OH G) CrO2, H2SO4, H2O Q) H30+ H) PCC, CH2Cl2 R) PBr3 1) Bre, hv S) H2, Pd J) heat T) CH2CH2CH2CH2OH, hea U) H20, H2SO4 Look at the given synthesis and the provided reagents. Fill in the blanks with the single...
e. 4-HC-C6H4-NH-C(O)-CH3 + Cl2/H4C-COH ------> H30* f. 4-nitro-1-chlorobenzene + NaOH H2O g. Ph-CH2-CH2-CH2-CO2H + AICI: ------->...
e. 4-HC-C6H4-NH-C(O)-CH3 + Cl2/H4C-COH ------> H30* f. 4-nitro-1-chlorobenzene + NaOH H2O g. Ph-CH2-CH2-CH2-CO2H + AICI: -------> h. All trans-H2C=CH-CH=CH-OCH3 + H2C=CH-C(O)-H i. 1-bromo-3-chlorobenzene + HNO3/H2SO4 j. CsH5-CH=CH-CH3 + HBr/peroxides --------> H30* k. Ph-CH2-CH3 + KMnO./NaOH/A ----------> L. CoHs-CCl3 + Bry/FeBr ---------- H30* m. Ph-Br + KNH/-33 °C --------
1) Name each of the following organic compounds: (a-b-c-e-f-g-j-k-I-m-n) a) CH3CH2CH2CH3 j) CH3CHBOCHBrCH3 b) CH3CH2CH2C(CH3)3 c)...
1) Name each of the following organic compounds: (a-b-c-e-f-g-j-k-I-m-n) a) CH3CH2CH2CH3 j) CH3CHBOCHBrCH3 b) CH3CH2CH2C(CH3)3 c) CH2=CHCH2CH2CH3 d) CH3CHCICH(CH3)2 k) CH2BrCH(CH3)CHCICH2CH3 1) CH2CH(OH)CH(CH3)2 m) (CH3)2CHCHO n) CH3CH2CH2COCH3 e) (CH3)2C(OH)CH2CH3 f) CH3CHO o) (CH3)2CHCOOH p) CH3CH2CN g) CH3CH2COCH2CH3 h) CH3CH2COOH 9) CH3CHBCH(OH)CH3 i) CH3CH(OH)CH2CHO r) CH3COCH(CH3)CHBCH3
Consider the SN2 reaction of butyl bromide with hydroxide ion , Assuming no other changes, what...
Consider the SN2 reaction of butyl bromide with hydroxide ion , Assuming no other changes, what effect on the reaction rate would result from simultaneously doubling the concentrations of both butyl bromide and hydroxyl ion No effect (B)It would double the rate (C)it would increase the rate six times (D) It would increase the rate four times. 2. Which alky halide would you expect to undergo SN1 hydrolysis most rapidly? (A) (CH3)3C-I (B) (CH3)3C-Br (C) (CH3)3C-Cl (D) (CH3)3C-F 3....
The two reactants shown below are combined to bring about a nucleophilic substitution reaction. CH3 + H2O Otos i. H30+ e. "OTos f. OH g. H2O h. "OS j. CH3OH k. none Which letter designates the electrophilic carbon at which substitution occurs? (If no reaction occurs enter the letter corresponding to "none.") Which letter corresponds to the leaving group? 1:1 1 .deicotill 1:1.00 Which letter corresponds to the leaving group? O Which letter designates the nucleophile?
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...
The two reactants shown below are combined to bring about a nucleophilic substitution reaction. F + Nal IT g. HI h. Nat i. none f. HF Which letter designates the electrophilic carbon at which substitution occurs? (If no reaction occurs enter the letter corresponding to "none.") Which letter corresponds to the leaving group? Which letter designates the nucleophile? Submit Answer Try Another Version 1 item attempt remaining
The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Which letter designates the electrophilic carbon at which substitution occurs? (If no reaction occurs enter the letter corresponding to "none.") Which letter corresponds to the leaving group? Which letter designates the nucleophile?
[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...
1) State which of the electrophiles given below will react
preferentially by i) SN1, ii) by SN2, or iii) capable of reacting
by either of the two mechanisms depending on the given conditions.
How can you affect those conditions to favour SN1 or SN2? Reason
your predictions based on the structures of the compounds. Br-CH3,
Br-CH2CH3, Br-CH(CH3)2, Br-C(CH3)3, Br-CH2-C5H6; C5H6 = phenyl
Introduction Alkyl halides can be prepared from alcohols by reactions with hydrogen halides (HCI, HBr, or HI) via...
Question 20 15 pts OH A) HBr K) Cl2, hv B) NaOH, H2O L) SOCI2 C) CH3COONa, DMF M) LiAIH4, THE D) CH3CH2CH2CH2MgBr, ether N) NaBH4, CH3CH2OH E) CH3CH2MgBr, ether O) CH3CH2OH, H2SO4 F) CH3CH2Li, ether P) CH3CH2ONa, CH2OH G) CrO2, H2SO4, H2O Q) H30+ H) PCC, CH2Cl2 R) PBr3 1) Bre, hv S) H2, Pd J) heat T) CH2CH2CH2CH2OH, hea U) H20, H2SO4 Look at the given synthesis and the provided reagents. Fill in the blanks with the single...
e. 4-HC-C6H4-NH-C(O)-CH3 + Cl2/H4C-COH ------> H30* f. 4-nitro-1-chlorobenzene + NaOH H2O g. Ph-CH2-CH2-CH2-CO2H + AICI: -------> h. All trans-H2C=CH-CH=CH-OCH3 + H2C=CH-C(O)-H i. 1-bromo-3-chlorobenzene + HNO3/H2SO4 j. CsH5-CH=CH-CH3 + HBr/peroxides --------> H30* k. Ph-CH2-CH3 + KMnO./NaOH/A ----------> L. CoHs-CCl3 + Bry/FeBr ---------- H30* m. Ph-Br + KNH/-33 °C --------
1) Name each of the following organic compounds: (a-b-c-e-f-g-j-k-I-m-n) a) CH3CH2CH2CH3 j) CH3CHBOCHBrCH3 b) CH3CH2CH2C(CH3)3 c) CH2=CHCH2CH2CH3 d) CH3CHCICH(CH3)2 k) CH2BrCH(CH3)CHCICH2CH3 1) CH2CH(OH)CH(CH3)2 m) (CH3)2CHCHO n) CH3CH2CH2COCH3 e) (CH3)2C(OH)CH2CH3 f) CH3CHO o) (CH3)2CHCOOH p) CH3CH2CN g) CH3CH2COCH2CH3 h) CH3CH2COOH 9) CH3CHBCH(OH)CH3 i) CH3CH(OH)CH2CHO r) CH3COCH(CH3)CHBCH3
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