Homework Answers
For each of the given pairs indicate which substance (A or B) will react faster in...
For each of the given pairs indicate which substance (A or B)
will react faster in an SN2 reaction by selecting the correct
compound from the dropdown menu. Then select the chemical principle
why that substance has a faster SN2 reaction.
Comparing Pair 1: Compound [ Select ] ["A",
"B", "both equal"] has a faster SN2 reaction due to [ Select
] ["a better leaving group", "a worse leaving group",
"more branches at the reacting carbon", "fewer branches at the
reacting...
For each of the given pairs indicate which substance (A or B) will react faster in...
For each of the given pairs indicate which substance (A or B)
will react faster in an SN2 reaction by selecting the correct
compound from the dropdown menu. Then select the chemical principle
why that substance has a faster SN2 reaction.
Comparing Pair 1: Compound [A,B,Both Equal] has
a faster SN2 reaction due to ["a better leaving group", "a worse
leaving group", "more branches at the reacting carbon", "fewer
branches at the reacting carbon", "more steric hindrance near the
leaving...
plus state the reason why the following nucleophile is better nucleophile from the reasons given in...
plus state the reason why the following nucleophile is
better nucleophile from the reasons given in pic.
Question 2 16 pts H2S vs. H2O A Pair 1 B VS. в OH Pair 2 VS. CI (protic solvent) OH A vs. H2O Pair 3 B Pair 4 " CH,CH NH2 vs. CH.CH OH Pair 5 B (aprotic solvent) A Pair 6 B NH2 o vs. Pair 7 F vs. M Pair 8 B A B For each of the given pairs...
2 Nered For each pair of compounds (a e), indicate the compound that will be faster...
2 Nered For each pair of compounds (a e), indicate the compound that will be faster in the given reaction. If the reaction rates should be approximately the same, indicate that instead. of 2.50 estion Compound A Compound B a or cho Br in E2 reaction CH) el CHE b. or in E2 reaction c. CI or in S, 2 reaction Br H H H Н. d. or in E2 reaction CH Br CH H H H H Br Br...
Need help answering this question Compound [A,B,Both Equal] has a faster SN2 reaction due to ["a...
Need help answering this question
Compound [A,B,Both Equal] has a faster SN2 reaction due to ["a
better leaving group", "a worse leaving group", "more branches at
the reacting carbon", "fewer branches at the reacting carbon",
"more steric hindrance near the leaving group", "less steric
hindrance near the leaving group", "some other reason"]
Comparing Pair 6: Compound [Select] is a better nucleophile due to [ Select] OBI A vs. Pair 6 Claprotic solvent) B.
And which reaction occurs faster Мар Consider the pair of reactions (1) and (2) below. (a)...
And which reaction occurs faster
Мар Consider the pair of reactions (1) and (2) below. (a) Predict the major organic and inorganic products of each reaction. (1) ^ NH2 DMSO 1 equiv. 1 equiv. (2) + DMSO B: 1 equiv. H2C-o: 1 equiv. (b) Determine whether the reactions will occur via the SN1, SN2, E1 or E2 mechanism. Select one below. O SNI continued below... OSN2 Ο Ε1 lo E2
Dropdown Menus: 1. methyl, primary (unhindered), primary (hindered), secondary, tertiary 2. poor, weakly basic, strong...
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
CH3CH2ONa ??? CH3CH2OH Br OH OH OH De on an or rega ang Look at the given reaction and select the most appropriate...
Dropdown Menus: 1. methyl, primary (unhindered), primary (hindered), secondary, tertiary 2. poor, weakly basic, strongly basic...
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
OH Hom 유 용 The Tone The ♡ ♡ Tñ y OH H OH E OH F HO3 G Look at the given...
Ignore the boxes with answers but question 18-32 I need help with there was a typo...
Ignore the boxes with answers but question 18-32 I need help
with
there was a typo with numbering
18. A sample contains mol of Both samples have the mode b. Both samples have them c. The Cumple has a smaller the d. The Fe sample contains fewer som ince the Te Which l to fais w ethan that of te imaofe is less than that of Select Response - Anwer Table please write your choices for 1-1 in this table...
Part 2 Multiple Choice. Select the best answer for each of the questions below: 1. Which...
Part 2 Multiple Choice. Select the best answer for each of the questions below: 1. Which of these molecules is not an electrophile? a) CH4 b) CH3+ c) H* d) BF3 2. Which of these molecules is not a nucleophile ? a) NH3 b) OH c) CN d) H* 3. Water behaves as: a) a nucleophile b) an electrophile c) both d) neither 4. The SN2 reaction has how many steps? a) 1 b) 2 c) 3 d) 4 5....
For each of the given pairs indicate which substance (A or B)
will react faster in an SN2 reaction by selecting the correct
compound from the dropdown menu. Then select the chemical principle
why that substance has a faster SN2 reaction.
Comparing Pair 1: Compound [ Select ] ["A",
"B", "both equal"] has a faster SN2 reaction due to [ Select
] ["a better leaving group", "a worse leaving group",
"more branches at the reacting carbon", "fewer branches at the
reacting...
For each of the given pairs indicate which substance (A or B)
will react faster in an SN2 reaction by selecting the correct
compound from the dropdown menu. Then select the chemical principle
why that substance has a faster SN2 reaction.
Comparing Pair 1: Compound [A,B,Both Equal] has
a faster SN2 reaction due to ["a better leaving group", "a worse
leaving group", "more branches at the reacting carbon", "fewer
branches at the reacting carbon", "more steric hindrance near the
leaving...
plus state the reason why the following nucleophile is
better nucleophile from the reasons given in pic.
Question 2 16 pts H2S vs. H2O A Pair 1 B VS. в OH Pair 2 VS. CI (protic solvent) OH A vs. H2O Pair 3 B Pair 4 " CH,CH NH2 vs. CH.CH OH Pair 5 B (aprotic solvent) A Pair 6 B NH2 o vs. Pair 7 F vs. M Pair 8 B A B For each of the given pairs...
2 Nered For each pair of compounds (a e), indicate the compound that will be faster in the given reaction. If the reaction rates should be approximately the same, indicate that instead. of 2.50 estion Compound A Compound B a or cho Br in E2 reaction CH) el CHE b. or in E2 reaction c. CI or in S, 2 reaction Br H H H Н. d. or in E2 reaction CH Br CH H H H H Br Br...
Need help answering this question
Compound [A,B,Both Equal] has a faster SN2 reaction due to ["a
better leaving group", "a worse leaving group", "more branches at
the reacting carbon", "fewer branches at the reacting carbon",
"more steric hindrance near the leaving group", "less steric
hindrance near the leaving group", "some other reason"]
Comparing Pair 6: Compound [Select] is a better nucleophile due to [ Select] OBI A vs. Pair 6 Claprotic solvent) B.
And which reaction occurs faster
Мар Consider the pair of reactions (1) and (2) below. (a) Predict the major organic and inorganic products of each reaction. (1) ^ NH2 DMSO 1 equiv. 1 equiv. (2) + DMSO B: 1 equiv. H2C-o: 1 equiv. (b) Determine whether the reactions will occur via the SN1, SN2, E1 or E2 mechanism. Select one below. O SNI continued below... OSN2 Ο Ε1 lo E2
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
CH3CH2ONa ??? CH3CH2OH Br OH OH OH De on an or rega ang Look at the given reaction and select the most appropriate...
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
OH Hom 유 용 The Tone The ♡ ♡ Tñ y OH H OH E OH F HO3 G Look at the given...
Ignore the boxes with answers but question 18-32 I need help
with
there was a typo with numbering
18. A sample contains mol of Both samples have the mode b. Both samples have them c. The Cumple has a smaller the d. The Fe sample contains fewer som ince the Te Which l to fais w ethan that of te imaofe is less than that of Select Response - Anwer Table please write your choices for 1-1 in this table...
Part 2 Multiple Choice. Select the best answer for each of the questions below: 1. Which of these molecules is not an electrophile? a) CH4 b) CH3+ c) H* d) BF3 2. Which of these molecules is not a nucleophile ? a) NH3 b) OH c) CN d) H* 3. Water behaves as: a) a nucleophile b) an electrophile c) both d) neither 4. The SN2 reaction has how many steps? a) 1 b) 2 c) 3 d) 4 5....
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