Homework Answers
In SN1 reaction polar protic solvent is used because here solvent act as nucleophile.
Hence correct answer is option D i.e. SN1 , CH3OH
Add Answer to:
HCI Choose the correct mechanism and then the solvent that is best for the reaction. CH3OH...
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...
What is the major Organic product expected from the following reaction? ОН Онө СІ CH3CH2OH ОН...
What is the major Organic product expected from the following reaction? ОН Онө СІ CH3CH2OH ОН ОСН-СН; Н;CH,CO СІ (c) (b) ОН (d) (е) Оа, а Ob.b Ос. с Od.d O e.e f. f What is the best route for converting the alcohol to the ether as shown below using a substitution reaction or a sequence of substitution reactions while preserving the stereochemistry at the chiral OH OCH a LICH b.i.HCI; ii. CH3OH Оe NaoCH3 d. CH3OH Oei. HCI; NaOCH...
20. Arrange the following molecules based on their reactivity for SN1 mechanism (the most reactive to...
20. Arrange the following molecules based on their reactivity for SN1 mechanism (the most reactive to the least reactive) [4pts] Br Br CH3Br Br 21. Considering the SN1, SN2, E1, and E2 mechanisms, the energy diagram shown below corresponds to [4Pts] a. only the SN1 mechanism b. only the E1 mechanism c. both the SN2 and E2 mechanisms d. only the SN2 mechanism. e. only the E2 mechanism f. both the SN1 and El mechanisms energy rxn coordinate 22. If...
Which of the following nucleophiles, in conjunction with heat and water as a byproduct, is most...
Which of the following nucleophiles, in conjunction with heat and
water as a byproduct, is most probable in the following
substitution reaction and by which mechanism?
CH нс— сн, CI CH Н,с- сн, Он 8о OH20, SN1 CH30", SN2 HI, SN2 HCI, SN1 OH, SN1
3) Write a complete Sn1 mechanism for the following reaction Also, 4) Write a complete Sn2...
3) Write a complete Sn1 mechanism for the following
reaction
Also,
4) Write a complete Sn2 mechanism for the following.
Please show transition state and list a good solvent as well.
Thank you!
3. Write a complete Sn1 mechanism for the following reaction. Вт + CH3OH CH₃CH2 CH3 4. Write a complete SN2 mechanism for the following. Show the transition state as well. Also list a good solvent. OTS + NaCN H3C 3. Write a complete sul mechanism for the...
3. (continued) For each reaction, draw the structure of the major product(s) including stereochemistry where appropriate....
3. (continued) For each reaction, draw the structure of the major product(s) including stereochemistry where appropriate. Fill in the box below each arrow with the mechanism(s) that will be followed (SN1/E1, SN2, or E2). For SN1/E1 reactions, draw products for both. g) Сн,сн,он h) CH2O- Na CH3OH i) Me. Br A Eto Nat Me
Provide a mechanism with arrows of this reaction b) In our reaction, which factors create conditions...
Provide a mechanism with
arrows of this reaction
b) In our reaction, which factors create conditions favorable
for an SN1 mechanism, which
factor(s) suggest that the mechanism might prefer an SN2
mechanism?
HO-6 но но но-s Camphor-10-sulfonic MW 232.30 он он OCH3 OCH3 4-Methoxybenzaldehyde Methyl α-D-gluco- pyranoside GlcMe MW 194.2 DMSO Axial position of OCH3 group dimethyl acetal acid (racemic) on C-1 indicates a-configuration MW 312 MW 182.2 bp 235 °C den. 1.068 solvent mp 167 - 168 °C mp...
(S)-3-Chlorooctane m DMSO S SN2 Factors Nucleophile Strength Leaving Group Solvent d) Cla . NaBrº DMSO...
(S)-3-Chlorooctane m DMSO S SN2 Factors Nucleophile Strength Leaving Group Solvent d) Cla . NaBrº DMSO Syl SN2 Factors Nucleophile Strength Leaving Group Solvent SN1 and SN2 Reactions 1. For each of the following reactions • Provide a complete detailed mechanism and predict the products. Indicate if the reaction proceeds via a Snl or Sn2 mechanism • Include the specific stereochemistry where appropriate.
Predict the major product for the following reaction. Label whether the reaction will proceed through an...
Predict the major product for the following reaction. Label whether the reaction will proceed through an SN2, Sn1, E2, or E1 mechanism. SN2 / S1/E2/E1 сн. Br NaCN (1 mol) (1 mol) Predict the major product for the following reaction. Label whether the reaction will proceed through an SN2, SN1, E2, or E1 mechanism. SN27 SN1/E2/E1 NaOCH; Сн,он Draw the line structures of the reactants below and predict the product of their reaction. Label the reaction as SN1, SN2, E1,...
Which mechanism is most likely for the reaction shown? (More than one choice may be possible)...
Which mechanism is most likely for the reaction shown? (More than one choice may be possible) SN2 BSN1 Radical Addition Br2 (1 equiv.) CsHg 1 h at 80 °C light Which mechanism is most likely for the reaction shown? (More than one choice may be possible) SN2 B SN1 Radical Addition NaCN DMF 50 °C Which mechanism is most likely for the reaction shown? (More than one choice may be possible) SN2 SN1 D Radical Addition Сн,ОН K2CO3 100 °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...
What is the major Organic product expected from the following reaction? ОН Онө СІ CH3CH2OH ОН ОСН-СН; Н;CH,CO СІ (c) (b) ОН (d) (е) Оа, а Ob.b Ос. с Od.d O e.e f. f What is the best route for converting the alcohol to the ether as shown below using a substitution reaction or a sequence of substitution reactions while preserving the stereochemistry at the chiral OH OCH a LICH b.i.HCI; ii. CH3OH Оe NaoCH3 d. CH3OH Oei. HCI; NaOCH...
20. Arrange the following molecules based on their reactivity for SN1 mechanism (the most reactive to the least reactive) [4pts] Br Br CH3Br Br 21. Considering the SN1, SN2, E1, and E2 mechanisms, the energy diagram shown below corresponds to [4Pts] a. only the SN1 mechanism b. only the E1 mechanism c. both the SN2 and E2 mechanisms d. only the SN2 mechanism. e. only the E2 mechanism f. both the SN1 and El mechanisms energy rxn coordinate 22. If...
Which of the following nucleophiles, in conjunction with heat and
water as a byproduct, is most probable in the following
substitution reaction and by which mechanism?
CH нс— сн, CI CH Н,с- сн, Он 8о OH20, SN1 CH30", SN2 HI, SN2 HCI, SN1 OH, SN1
3) Write a complete Sn1 mechanism for the following
reaction
Also,
4) Write a complete Sn2 mechanism for the following.
Please show transition state and list a good solvent as well.
Thank you!
3. Write a complete Sn1 mechanism for the following reaction. Вт + CH3OH CH₃CH2 CH3 4. Write a complete SN2 mechanism for the following. Show the transition state as well. Also list a good solvent. OTS + NaCN H3C 3. Write a complete sul mechanism for the...
3. (continued) For each reaction, draw the structure of the major product(s) including stereochemistry where appropriate. Fill in the box below each arrow with the mechanism(s) that will be followed (SN1/E1, SN2, or E2). For SN1/E1 reactions, draw products for both. g) Сн,сн,он h) CH2O- Na CH3OH i) Me. Br A Eto Nat Me
Provide a mechanism with
arrows of this reaction
b) In our reaction, which factors create conditions favorable
for an SN1 mechanism, which
factor(s) suggest that the mechanism might prefer an SN2
mechanism?
HO-6 но но но-s Camphor-10-sulfonic MW 232.30 он он OCH3 OCH3 4-Methoxybenzaldehyde Methyl α-D-gluco- pyranoside GlcMe MW 194.2 DMSO Axial position of OCH3 group dimethyl acetal acid (racemic) on C-1 indicates a-configuration MW 312 MW 182.2 bp 235 °C den. 1.068 solvent mp 167 - 168 °C mp...
(S)-3-Chlorooctane m DMSO S SN2 Factors Nucleophile Strength Leaving Group Solvent d) Cla . NaBrº DMSO Syl SN2 Factors Nucleophile Strength Leaving Group Solvent SN1 and SN2 Reactions 1. For each of the following reactions • Provide a complete detailed mechanism and predict the products. Indicate if the reaction proceeds via a Snl or Sn2 mechanism • Include the specific stereochemistry where appropriate.
Predict the major product for the following reaction. Label whether the reaction will proceed through an SN2, Sn1, E2, or E1 mechanism. SN2 / S1/E2/E1 сн. Br NaCN (1 mol) (1 mol) Predict the major product for the following reaction. Label whether the reaction will proceed through an SN2, SN1, E2, or E1 mechanism. SN27 SN1/E2/E1 NaOCH; Сн,он Draw the line structures of the reactants below and predict the product of their reaction. Label the reaction as SN1, SN2, E1,...
Which mechanism is most likely for the reaction shown? (More than one choice may be possible) SN2 BSN1 Radical Addition Br2 (1 equiv.) CsHg 1 h at 80 °C light Which mechanism is most likely for the reaction shown? (More than one choice may be possible) SN2 B SN1 Radical Addition NaCN DMF 50 °C Which mechanism is most likely for the reaction shown? (More than one choice may be possible) SN2 SN1 D Radical Addition Сн,ОН K2CO3 100 °C...
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