The following rate law could be possible for which of the following mechanisms?
E1 |
E2 |
SN1 |
SN2 |
E2 and SN2 |
The rate law for the above shown equation is both E2 and SN2
But, little clarification on use of diisopropylamine.
If diisopropylamine in above reaction is acts as nucleophile then that comes under SN2 reaction.
If diisopropylamine in above reaction is acts as base than that comes under E2 reaction.
If both base and nucleophile then it is both E2 and Sn2 reactions
E1 and SN1 rate law = K [aryl/alkyl-X]
The following rate law could be possible for which of the following mechanisms? E1 E2 SN1...
The following rate law could be possible for which of the following mechanisms? Rate = k Ο Ε1 OSN2 E2 & SN2 E2 SNI
Find the products, and specify which mechanisms used, SN1, SN2, E1, E2 ? We were unable to transcribe this imageWe were unable to transcribe this imageHzC CI ОК он Fill in the Blank with a possible Produc
will this reaction be SN2, SN1, E1 or E2? draw possible products and label the major if applicable please and thank you! - - - will this non be SN2, SNI , El or E2? @ then, drow possible products and label the major (if applicable) H2O
Thermodynamics and kinetics of SN1, SN2, E1, and E2 mechanisms. 2. Draw the reaction coordinate diagrams of the following reactions according to the type of mechanisms given and include the following: a) Label the reactant, product, intermediates, and a drawing of the transition state of the rate determining step. If there are multiple E, label the largest E (5 pts) b) State if AG rx is <0 or >0 and make sure your diagram reflects the AGxn. (4 pts) Hint:...
Consider the following statement regarding Sn1, Sn2, E1, E2 reactions. To which mechanism(s), if any, apply? 1.Rearrangements of the carbon skeleton are possible?
Circle the mechanism (SN2, SN1, E2, or E1) responsible for the formation of each product in this reaction. If the product cannot be formed in the reaction, circle "not a product". (2 pts) ГОН SN2 SN1 E2 E1 S N2 SN1 E2 E1 SN2 SN1 E2 E1 S2 Sn1 E2 E1 not a product not a product not a product not a product
н.W. 10-E2, E1, Sn1 and Sn2 Each substrate undergoes E2 elimination with NaOCHs. Draw the ß-hydrogens, then draw each possible elimination product, and identify the major isomer. The first is shown as an example. Notice he base is a strong base which promotes 2nd order mechanisms Br Br major No need to draw all beta-hydrogens if they are equivalent. minor NaOCH Br Br Br Br
Which reaction (Sn1, Sn2, E2, E1) will go through a cationic intermediate?
which substitution and elimination reactions follows Zaitsev’s rule? SN1, E1, SN2, E2?
Identify whether each of the following reactions occurs through an SN1, SN2, E1, or E2 mechanism. Identify whether each of the following reactions occurs through an Sn1 , Sn2, E1, or E2 mechanism.