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Please explain answers Use the reaction below to answer the three questions that follow: SNa DMSO...
Use the reaction below to answer the three questions that follow: SNa DMSO 16. What effect...
Use the reaction below to answer the three questions that follow: SNa DMSO 16. What effect would changing the nucleophile to ethoxide have on the rate of the reaction above? a. The rate would increase. C. The rate would decrease. b. There would be no reaction. d. No effect on rate would be observed. 17. What effect would changing the iodine atom to a chlorine atom have on the rate of the reaction? a. There would be no reaction. c....
Please explain with explanations tks a lot 1. (1S,2S)-1-iodo-2-methylcyclohexane + KOH/ H2S / DMSO --> 2....
Please explain with explanations tks a lot 1. (1S,2S)-1-iodo-2-methylcyclohexane + KOH/ H2S / DMSO --> 2. S-2-iodobutane + KF / MeOH --> 3. 1-iodopropane + sodium metal / ethanol --> 4. isopropyl alcohol + NaNH2 --> 5. 1-butene + HBr / peroxides --> 6. bromobutane + NaH / 1-pentanol --> 7. Which would proceed fastest via an SN2 reaction? a. 1-iodobutane + sodium ethoxide in DMSO b. 2-bromobutane + sodium cyanide in DMSO c. 2-methyl-2-chlorobutane + sodium ethoxide in DMSO d....
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...
Which statement or set of conditions listed below is not consistent with an Syl reaction pathway?...
Which statement or set of conditions listed below is not consistent with an Syl reaction pathway? O a. Neutral nucleophile work just fine. b. The leaving group is typically the conjugate base of a strong acid. O c. The rate is not dependent upon the concentration of the nucleophile. d. The temperature is relatively "cooler" to reduce competing elimination products. e. The solvent is polar and aprotic. Of. The substrate has a leaving group that is typically on a 30,...
Consider the SN2 reaction shown below and answer the following questions. Consider the SN1 reaction shown...
Consider the SN2 reaction shown below and answer the
following questions.
Consider the SN1 reaction shown below and answer the following
questions.
1. Consider the SN2 reaction shown below and answer the following questions. acetone Br NaSCH3 SCH3 NaBr + A. Write the rate law for the reaction B. Identify the nucleophile and the electrophile in the reaction C. State how each of the following factors would affect the rate of the reaction a. Increasing the concentration of 1-bromopropane. b....
1. Consider the SN2 reaction shown below and answer the following questions. acetone Br + NaSCHE...
1. Consider the SN2 reaction shown below and answer the following questions. acetone Br + NaSCHE SCHg+ NaBr A. Write the rate law for the reaction. B. Identify the nucleophile and the electrophile in the reaction. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of 1-bromopropane. b. Decreasing the concentration of NaSCH3 by one-half. c. Changing 1-bromopropane to 2-bromopropane. d. Changing 1-bromopropane to 1-iodopropane. e. Changing NaSCH3 to CH3OH.
1. Consider the SN2 reaction shown below and answer the following questions. acetone + NaSCHE SCH3...
1. Consider the SN2 reaction shown below and answer the following questions. acetone + NaSCHE SCH3 + NaBr A. Write the rate law for the reaction. B. Identify the nucleophile and the electrophile in the reaction. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of 1-bromopropane. b. Decreasing the concentration of NaSCH3 by one-half. C. Changing 1-bromopropane to 2-bromopropane. d. Changing 1-bromopropane to 1-iodopropane. e. Changing NaSCH3 to CH3OH.
1. Consider the SN2 reaction shown below and answer the following questions. Br + acetone NaSCH—...
1. Consider the SN2 reaction shown below and answer the following questions. Br + acetone NaSCH— ^ SCH3 + NaBr A. Write the rate law for the reaction. B. Identify the nucleophile and the electrophile in the reaction. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of 1-bromopropane. b. Decreasing the concentration of NaSCH3 by one-half. c. Changing 1-bromopropane to 2-bromopropane. d. Changing 1-bromopropane to 1-iodopropane. e. Changing NaSCH3...
please explain the work 1. Consider the S2 reaction between thioacetate anion and lodoethane in DMSO...
please explain the work
1. Consider the S2 reaction between thioacetate anion and lodoethane in DMSO at 25 °C. Holyo . moto elettrodom a. Which molecule (or ion) is serving as the nucleophile in this reaction? b. Which molecule (or ion) is serving as the electrophile in this reaction? c. Which molecule (or ion) is serving as the leaving group in this reaction? d. What is the rate law for this reaction? e. Draw curved arrows on the reactants to...
please explain why g. Consider the following reaction to answer the questions below. (4pts each) MC...
please explain why
g. Consider the following reaction to answer the questions below. (4pts each) MC CH3OH A) The reaction is likely to proceed via an mechanism. Circle your choice Sw1 S2 E1 E2 B) Would the rate of this reaction increase by switching the nucleophile to CH,O-? YES I NO (Circle one) C) In this reaction, the stereochemistry of the carbon bearing the leaving group would undergo RACEMIZATION / INVERSION / RETENTION of stereochemical configuration (Circle one)
Use the reaction below to answer the three questions that follow: SNa DMSO 16. What effect would changing the nucleophile to ethoxide have on the rate of the reaction above? a. The rate would increase. C. The rate would decrease. b. There would be no reaction. d. No effect on rate would be observed. 17. What effect would changing the iodine atom to a chlorine atom have on the rate of the reaction? a. There would be no reaction. c....
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...
Which statement or set of conditions listed below is not consistent with an Syl reaction pathway? O a. Neutral nucleophile work just fine. b. The leaving group is typically the conjugate base of a strong acid. O c. The rate is not dependent upon the concentration of the nucleophile. d. The temperature is relatively "cooler" to reduce competing elimination products. e. The solvent is polar and aprotic. Of. The substrate has a leaving group that is typically on a 30,...
Consider the SN2 reaction shown below and answer the
following questions.
Consider the SN1 reaction shown below and answer the following
questions.
1. Consider the SN2 reaction shown below and answer the following questions. acetone Br NaSCH3 SCH3 NaBr + A. Write the rate law for the reaction B. Identify the nucleophile and the electrophile in the reaction C. State how each of the following factors would affect the rate of the reaction a. Increasing the concentration of 1-bromopropane. b....
1. Consider the SN2 reaction shown below and answer the following questions. acetone Br + NaSCHE SCHg+ NaBr A. Write the rate law for the reaction. B. Identify the nucleophile and the electrophile in the reaction. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of 1-bromopropane. b. Decreasing the concentration of NaSCH3 by one-half. c. Changing 1-bromopropane to 2-bromopropane. d. Changing 1-bromopropane to 1-iodopropane. e. Changing NaSCH3 to CH3OH.
1. Consider the SN2 reaction shown below and answer the following questions. acetone + NaSCHE SCH3 + NaBr A. Write the rate law for the reaction. B. Identify the nucleophile and the electrophile in the reaction. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of 1-bromopropane. b. Decreasing the concentration of NaSCH3 by one-half. C. Changing 1-bromopropane to 2-bromopropane. d. Changing 1-bromopropane to 1-iodopropane. e. Changing NaSCH3 to CH3OH.
1. Consider the SN2 reaction shown below and answer the following questions. Br + acetone NaSCH— ^ SCH3 + NaBr A. Write the rate law for the reaction. B. Identify the nucleophile and the electrophile in the reaction. C. State how each of the following factors would affect the rate of the reaction. a. Increasing the concentration of 1-bromopropane. b. Decreasing the concentration of NaSCH3 by one-half. c. Changing 1-bromopropane to 2-bromopropane. d. Changing 1-bromopropane to 1-iodopropane. e. Changing NaSCH3...
please explain the work
1. Consider the S2 reaction between thioacetate anion and lodoethane in DMSO at 25 °C. Holyo . moto elettrodom a. Which molecule (or ion) is serving as the nucleophile in this reaction? b. Which molecule (or ion) is serving as the electrophile in this reaction? c. Which molecule (or ion) is serving as the leaving group in this reaction? d. What is the rate law for this reaction? e. Draw curved arrows on the reactants to...
please explain why
g. Consider the following reaction to answer the questions below. (4pts each) MC CH3OH A) The reaction is likely to proceed via an mechanism. Circle your choice Sw1 S2 E1 E2 B) Would the rate of this reaction increase by switching the nucleophile to CH,O-? YES I NO (Circle one) C) In this reaction, the stereochemistry of the carbon bearing the leaving group would undergo RACEMIZATION / INVERSION / RETENTION of stereochemical configuration (Circle one)
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