Homework Answers
(a) The IUPAC names of thr structure are given below.
- 1-Bromobutane
- 1-Chloro-2-methylcyclohexane.
- 2-Florobutane.
- 1-Bromo-1, 3- methylcyclohexane.
- 1,3-Difloro-2-iodopropane.
(b) The leaving group in the following structure respectively is given as
- -Cl
- -Cl
- -F
- -Br
- -I
(c) Degree of substitution means, how many carbons are attached to the carbon. It is given below respectively.
- 1 degree of substitution
- 2 degree of substitution
- 2 degree of substitution
- 3 degree of substitution
- 2 degree of substitution
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please answer question
For each of the following structures (a) Give the IUPAC name (b) Identify...
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group....
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3. (1) Identify the same carbon as in (c) and (d) in the product as (R) or (S), if applicable. (g) Choose the most appropriate solvent to facilitate...
please answer d e f g For each of the following structures: (a) Give the IUPAC...
please answer d e f g
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3- (1) Identify the same carbon as in (c) and (d) in the product as (R) or (S), if applicable. (g) Choose...
for the following SN1 reaction draw the major organic product identify the nucleophile substrate and and...
for the following SN1 reaction draw the major organic product
identify the nucleophile substrate and and leaving group and
determine the rate limiting step
Organic Chemistry (solvent) 0 H2O is the substrate, C,HeBr is the nucleophile, and Br is the leaving group
For the following Sn1 reaction, draw the major organic product, identify the nucleophile, substrate, and leaving...
For the following Sn1 reaction, draw the major organic product, identify the nucleophile, substrate, and leaving group, and determine the rate limiting step. Нас ma H20 (solvent) Нас CHE Select the statement that properly identifies the nucleophile, substrate, and leaving group, O Br is the substrate, CyH5Br is the nucleophile, and H20 is the leaving group. 0 H2O is the substrate, C7H15Br is the nucleophile, and Br is the leaving group. O C7H15Br is the substrate, H20 is the nucleophile,...
For the following three structures, (a) identify the leaving group, LG, by circling it, and (b)...
For the following three structures, (a) identify the leaving
group, LG, by circling it, and (b) provide the substitution at the
alpha carbon, αC, by designating it as either unsubstituted, 1°,
2°, or 3°.
Apply the designated mechanism to the provided substrate and
nucleophile to predict the product(s).
For the following three structures, (a) identify the leaving group, LG, by circling it, and (b) provide the substitution at the alpha carbon, aC, by designating it as either unsubstituted, 1°, 2°,...
Choose the best answer for the main type of reaction shown below: For an SN2 reaction, the BEST scenario would be: Selec...
Choose the best answer for the main type of reaction shown
below:
For an SN2 reaction, the BEST scenario would be:
Select the term that best identifies relationship between the
two molecules shown.
Choose the best answer for the main type of reaction shown below: (1 mark) EtOH a) b) 2° alkylhalide, Syl reaction, one product 2° haloalkane, Syl reaction, racemic products 2º haloalkane, Sn1/E1 reactions, racemic products and alkene products 2º haloalkane, Sn2 reaction, one product 2° alkylhalide, Sn2...
30. What is wrong with the following mechanism? 33. Give the name(s) of the product(s) for...
30. What is wrong with the following mechanism? 33. Give the name(s) of the product(s) for the following SN2 reaction. Br Br A. There is no leaving group, so there B. The arrow should be removing a proton C. An arrow is also needed to indicate the D. The arrow indicating the formation of should be no arrows. from the H2O group. loss of the leaving group. the C-Br bond (nucleophilic attack) A) (S)-2-hexanol B) (R)-2-hexanol C) (S)-3-hexanol D) (R)-3-hexanol...
[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...
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...
1. Write the predicted product and the rate law for the following reaction: CH;CH CH CI...
1. Write the predicted product and the rate law for the following reaction: CH;CH CH CI + NaCN DMSO 2. In the following reaction, identify a) the leaving group, b) the nucleophile, c) the electrophilic carbon and d) the solvent CH CH Br + NaHS H30 CH CH SH + NaBr 3. Write out the reaction of (R)-2-bromopentane with sodium cyanide in DMSO, including the predicted major product: 4. Rank the following in decreasing order of leaving group ability (with...
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3. (1) Identify the same carbon as in (c) and (d) in the product as (R) or (S), if applicable. (g) Choose the most appropriate solvent to facilitate...
please answer d e f g
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3- (1) Identify the same carbon as in (c) and (d) in the product as (R) or (S), if applicable. (g) Choose...
for the following SN1 reaction draw the major organic product
identify the nucleophile substrate and and leaving group and
determine the rate limiting step
Organic Chemistry (solvent) 0 H2O is the substrate, C,HeBr is the nucleophile, and Br is the leaving group
For the following Sn1 reaction, draw the major organic product, identify the nucleophile, substrate, and leaving group, and determine the rate limiting step. Нас ma H20 (solvent) Нас CHE Select the statement that properly identifies the nucleophile, substrate, and leaving group, O Br is the substrate, CyH5Br is the nucleophile, and H20 is the leaving group. 0 H2O is the substrate, C7H15Br is the nucleophile, and Br is the leaving group. O C7H15Br is the substrate, H20 is the nucleophile,...
For the following three structures, (a) identify the leaving
group, LG, by circling it, and (b) provide the substitution at the
alpha carbon, αC, by designating it as either unsubstituted, 1°,
2°, or 3°.
Apply the designated mechanism to the provided substrate and
nucleophile to predict the product(s).
For the following three structures, (a) identify the leaving group, LG, by circling it, and (b) provide the substitution at the alpha carbon, aC, by designating it as either unsubstituted, 1°, 2°,...
Choose the best answer for the main type of reaction shown
below:
For an SN2 reaction, the BEST scenario would be:
Select the term that best identifies relationship between the
two molecules shown.
Choose the best answer for the main type of reaction shown below: (1 mark) EtOH a) b) 2° alkylhalide, Syl reaction, one product 2° haloalkane, Syl reaction, racemic products 2º haloalkane, Sn1/E1 reactions, racemic products and alkene products 2º haloalkane, Sn2 reaction, one product 2° alkylhalide, Sn2...
30. What is wrong with the following mechanism? 33. Give the name(s) of the product(s) for the following SN2 reaction. Br Br A. There is no leaving group, so there B. The arrow should be removing a proton C. An arrow is also needed to indicate the D. The arrow indicating the formation of should be no arrows. from the H2O group. loss of the leaving group. the C-Br bond (nucleophilic attack) A) (S)-2-hexanol B) (R)-2-hexanol C) (S)-3-hexanol D) (R)-3-hexanol...
[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...
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...
1. Write the predicted product and the rate law for the following reaction: CH;CH CH CI + NaCN DMSO 2. In the following reaction, identify a) the leaving group, b) the nucleophile, c) the electrophilic carbon and d) the solvent CH CH Br + NaHS H30 CH CH SH + NaBr 3. Write out the reaction of (R)-2-bromopentane with sodium cyanide in DMSO, including the predicted major product: 4. Rank the following in decreasing order of leaving group ability (with...
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