Althought epoxides do not contain a good leaving group, they contains a strained three membered ring with polar bonds. Nucleophilic attack opens the strained three membered ring making it favorable process even with the poor leaving group. This reaction occurs readily with strong nucleophilic , and with acids like HZ, where Z is nucleophilic atom. What would be the major product of reaction?A. B. C. D.

Althought epoxides do not contain a good leaving group, they contains

1.	Althought epoxides do not contain a good leaving group, they contains a strained three membered ring with polar bonds. Nucleophilic attack opens the strained three membered ring making it favorable process even with the poor leaving group. This reaction occurs readily with strong nucleophilic , and with acids like HZ, where Z is nucleophilic atom. What would be the major product of reaction?A. B. C. D.
Answer» Correct Answer - C

Discussion

No Comment Found

Related InterviewSolutions

An organic compound A (Molecular formula `C_(6)H_(12)O_(4))` on treatment with Na metal liberates `H_(2)` gas and on treatment with `HIO_(4)` gives 2 moles of `CH_(3)CHO,HCOOH(1"mole")and CO_(2)(1"mole")`. Find the structure on A.A. B. C. D.
The releative rate or acid catalyssed dehydration of following alcohols would be: (P) `Ph-overset(CH_(3))overset(|)(C)-underset(OH)underset(|)(CH)-CH_(3)` (Q) `Ph-overset(CH_(3))overset(|)(C)-CH_(2)-CH_(2)-OH` (R ) `Ph--underset(OH)underset(|)overset(CH_(3))overset(|)(CH)-CH_(2)CH_(3)` `Ph--underset(CH_(3))underset(|)overset(CH_(3))overset(|)(CH)-CH_(2)OH`A. `R gt P gt S gt Q`B. `R gt S gt P gt Q`C. `P gt R gt S gt Q`D. `R gt S gt Q gt P`
-OH group is substituted by -Br. The slowest step is dehydration. Which of the following is correct comparison of rate constant `K_(1) and K_(2)`?A. `k_(1)=k_(2)`B. `k_(1)gtk_(2)`C. `k_(1)ltk_(2)`D. cannot be predict
The releative rate or acid catalyssed dehydration of following alcohols would be: (P) `Ph-overset(CH_(3))overset(|)(C)-underset(OH)underset(|)(CH)-CH_(3)` (Q) `Ph-overset(CH_(3))overset(|)(C)-CH_(2)-CH_(2)-OH` (R ) `Ph--underset(OH)underset(|)overset(CH_(3))overset(|)(CH)-CH_(2)CH_(3)` `Ph--underset(CH_(3))underset(|)overset(CH_(3))overset(|)(CH)-CH_(2)OH`A. `R gt P gt S ge Q`B. `R gt S gt P gt Q`C. `P gt R gt S gt Q`D. `R gt S gt Q gt P`
An organic compound A (Molecular formula `C_(6)H_(12)O_(4))` on treatment with Na metal liberates `H_(2)` gas and on treatment with `HIO_(4)` gives 2 moles of `CH_(3)CHO,HCOOH(1"mole")and CO_(2)(1"mole")`. Find the structure on A.A. B. C. D.
Identify the major product of the following reation: A. B. C. D. No reaction
-OH group is substituted by -Br. The slowest step is dehydration. Which of the following is correct comparison of rate constant `K_(1) and K_(2)`?A. `k_(1)=k_(2)`B. `k_(1)gtk_(2)`C. `k_(1)ltk_(2)`D. cannot be predict
Consider the following sequence of reactions A. B. C. D.
The product A and B respectively:A. B. C. D.
Consider the following sequence of reactions A. B. C. D. `(+-)-2` butanol

Discussion

No Comment Found

Related InterviewSolutions

Reply to Comment