Arrange the haloalkanes in
order of increasing reactivity in an Sn2 reaction with NaI in
acetone (least first).
Homework Answers
ANSWER:-
the correct answer is d because we know that in SN2 reaction mechanism we use primary and secondary halides so III is least reactive because of its tertiary nature and we also know that the reactivity of Cl is less than that of Bromine and iodine so II is next least reactive IV is secondary carbocation so next reactivity is IV and I is most reactive because of primary carbocation.
ANSWER:-
the correct answer is d because we know that in SN2 reaction mechanism we use primary and secondary halides so III is least reactive because of its tertiary nature and we also know that the reactivity of Cl is less than that of Bromine and iodine so II is next least reactive IV is secondary carbocation so next reactivity is IV and I is most reactive because of primary carbocation.
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Arrange the haloalkanes in
order of increasing reactivity in an Sn2 reaction with NaI in
acetone...
1. arrange Alkyl chlorides in theoretical order of reactivity in SN1 reaction 2. arrange Alkyl chlorides in theoretica...
1. arrange Alkyl chlorides in theoretical order of reactivity
in SN1 reaction
2. arrange Alkyl chlorides in theoretical order of reactivity
in SN2 reaction
a HC 1-Chlorobutane AgNO3+ Ethanol (SN1) Nal + Acetone SN2 CH3 H3C 2-Chlorobutane Br CH3 H3C 2-Bromobutane CH3 H2C- a CH3 t-butylchloride Benzylchloride Br Bromobenzene
1. arrange Alkyl bromides in theoretical order of reactivity in SN1 reaction 2. arrange Alkyl bromides in theoretical o...
1.
arrange Alkyl bromides in theoretical order of reactivity in SN1
reaction
2. arrange Alkyl bromides in theoretical order of reactivity
in SN2 reaction
AgNO3+ Ethanol Yal H₂C (SN 1) 1-Chlorobutane Nal + Acetone SN2 CH3 H3C 2-Chlorobutane Br CH3 H3C 2-Bromobutane CH3 H2C- a CH3 t-butylchloride Benzylchloride Br Bromobenzene
2.Data Table. Arrange the alkyl halides from Figure 3 in the order of expected reactivity (most reactive first) in...
2.Data Table. Arrange the alkyl halides from Figure 3 in the order of expected reactivity (most reactive first) in EtOH/AgNO. Repeat the process for acetone/NaI. In both rankings, represent the molecules with both skeletal structures and name. Don't forget to include non-bonded electrons. D.OUTLA n-butyl chloride sec-butyl chloride tert-butyl chloride isobutyl chloride Вг. Br crotyl chloride n-butyl bromide ethyl iodide sec-butyl bromide
2. Arrange the following in order of: (i) increasing reactivity with HCI. CH, CH CH H.C=C...
2. Arrange the following in order of: (i) increasing reactivity with HCI. CH, CH CH H.C=C nec nec 20 cm H.C=C CH HC=C CH, (b) H.C=C NHCH, CHOCH, ОСН, (a) (c) (d) Teast reactive most reactive (ii) increasing stability. CH CH3 CH (a) (C) least stable most stable (iii) increasing heat of hydrogenation. CH,CH, CH=CH2 C H.CH O CH.CH CH3 CH,CH; CH,CH, (0) lowest heat of hydrogenation
Select the order that has the following nucleophiles correctly arranged with respect to increasing reactivity tow...
Select the order that has the following nucleophiles correctly arranged with respect to increasing reactivity tow following substitution reaction Question 4 Nu: Nu Br DMF CHCоо CH3O CHзон 2 3 3 12 2 1 3 1 2 3 1 3 2 2 3 1 3 2 1 B increasing reactivity increasing C increasing reactivity increasing A increasing reactivity increasing D reactivity reactivity reactivity Ов O F Enter Your Answer: A D Choose the major product(s) of the following reaction Question...
2 Number the co mpounds below in order of increasing reactivity towards Sn2 reaction. Br Cl...
2 Number the co mpounds below in order of increasing reactivity towards Sn2 reaction. Br Cl Circle the more nucleophilic of the two species below. CII,S) CI,SII Predict the product(s) of the reactions below, showing stereochemistry of the product and the starting halide CN Br S CH3 CN CH3S
( 4 ) Arrange the following carbocations in the order of increasing stability (least stable first)....
( 4 ) Arrange the following carbocations in the order of increasing stability (least stable first). СНа OC-CHE H-C-H N - a) IV, I, III, II b) III, I, IV, !! c) III, IV, II, 1 d) I, II, II, I
1. Rank the alkyl halides in each group in order of increasing E2 reactivity. a. Br...
1. Rank the alkyl halides in each group in order of increasing E2 reactivity. a. Br Br Br I П III b. Cн, Br Нас CI CH3 П III Rank the alkyl halides in each group of problem one in order of increasing El reactivity. 2. Which elimination reaction in each pair is faster? (I or II) 3. а. сн, Нас. Он Он II. b. HO DMSO он (CH),CCI (CH),CCI П. I. Н.о What alkenes are formed from each alkyl...
21. Rank the following dienes in order of increasing reactivity in a Diels-Alder reaction, listing the...
21. Rank the following dienes in order of increasing reactivity in a Diels-Alder reaction, listing the least reactive first. A. I II III B. III <I<II C. II <I<III D. I<III <II
Can you explain how to arrange these compounds in order of increasing boiling point. I. CH3...
Can you explain how to arrange these compounds in order of increasing boiling point. I. CH3 CH2 CH2 CH2 CH3 II. CH3 CH2 CH2 -O-CH3 III. CH3 CH2 CH2 CH2 OH IV. CH3 CH2 CH2 CHO and also how to arrange these compounds in order of decreasing melting point and in deceasing order of water solubility I. (CH3 ) 3 CH2 CH2 CH2 OH II. (CH3 ) 3 CCOOH III. (CH3 ) 2 CHCOOK
1. arrange Alkyl chlorides in theoretical order of reactivity
in SN1 reaction
2. arrange Alkyl chlorides in theoretical order of reactivity
in SN2 reaction
a HC 1-Chlorobutane AgNO3+ Ethanol (SN1) Nal + Acetone SN2 CH3 H3C 2-Chlorobutane Br CH3 H3C 2-Bromobutane CH3 H2C- a CH3 t-butylchloride Benzylchloride Br Bromobenzene
1.
arrange Alkyl bromides in theoretical order of reactivity in SN1
reaction
2. arrange Alkyl bromides in theoretical order of reactivity
in SN2 reaction
AgNO3+ Ethanol Yal H₂C (SN 1) 1-Chlorobutane Nal + Acetone SN2 CH3 H3C 2-Chlorobutane Br CH3 H3C 2-Bromobutane CH3 H2C- a CH3 t-butylchloride Benzylchloride Br Bromobenzene
2.Data Table. Arrange the alkyl halides from Figure 3 in the order of expected reactivity (most reactive first) in EtOH/AgNO. Repeat the process for acetone/NaI. In both rankings, represent the molecules with both skeletal structures and name. Don't forget to include non-bonded electrons. D.OUTLA n-butyl chloride sec-butyl chloride tert-butyl chloride isobutyl chloride Вг. Br crotyl chloride n-butyl bromide ethyl iodide sec-butyl bromide
2. Arrange the following in order of: (i) increasing reactivity with HCI. CH, CH CH H.C=C nec nec 20 cm H.C=C CH HC=C CH, (b) H.C=C NHCH, CHOCH, ОСН, (a) (c) (d) Teast reactive most reactive (ii) increasing stability. CH CH3 CH (a) (C) least stable most stable (iii) increasing heat of hydrogenation. CH,CH, CH=CH2 C H.CH O CH.CH CH3 CH,CH; CH,CH, (0) lowest heat of hydrogenation
Select the order that has the following nucleophiles correctly arranged with respect to increasing reactivity tow following substitution reaction Question 4 Nu: Nu Br DMF CHCоо CH3O CHзон 2 3 3 12 2 1 3 1 2 3 1 3 2 2 3 1 3 2 1 B increasing reactivity increasing C increasing reactivity increasing A increasing reactivity increasing D reactivity reactivity reactivity Ов O F Enter Your Answer: A D Choose the major product(s) of the following reaction Question...
2 Number the co mpounds below in order of increasing reactivity towards Sn2 reaction. Br Cl Circle the more nucleophilic of the two species below. CII,S) CI,SII Predict the product(s) of the reactions below, showing stereochemistry of the product and the starting halide CN Br S CH3 CN CH3S
( 4 ) Arrange the following carbocations in the order of increasing stability (least stable first). СНа OC-CHE H-C-H N - a) IV, I, III, II b) III, I, IV, !! c) III, IV, II, 1 d) I, II, II, I
1. Rank the alkyl halides in each group in order of increasing E2 reactivity. a. Br Br Br I П III b. Cн, Br Нас CI CH3 П III Rank the alkyl halides in each group of problem one in order of increasing El reactivity. 2. Which elimination reaction in each pair is faster? (I or II) 3. а. сн, Нас. Он Он II. b. HO DMSO он (CH),CCI (CH),CCI П. I. Н.о What alkenes are formed from each alkyl...
21. Rank the following dienes in order of increasing reactivity in a Diels-Alder reaction, listing the least reactive first. A. I II III B. III <I<II C. II <I<III D. I<III <II
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