Consider the following reaction
NaOEt
------>
EtOH
a) Identify the mechanism(s) by which the reaction will occur. If there is more than one mechanism that can operate, identify the mechanism that will predominate. Explain your reasoning clearly.
b) Predict all possible product(s) that will be formed and identify them as major and minor products.
Solution:
A) The mechanism and three products are given below.
B) Elimination produces major product due to stability of transitiin state, while substitution produces minor product.
Consider the following reaction NaOEt EtOH a) Identify the mechanism(s) by which the reaction will occur....
Predict the products and provide the complete arrow-pushing mechanism for the reaction below. NaOEt EtOH
(1) 07.76 c : Minor ONLY (2) 07.76 e: Minor ONLY (3) 07.76 f: Major and Minor (4) 07.76 h: Minor ONLY (5) 07.76 i: Minor ONLY (6) 07.76 j: Minor ONLY Practice Problem 07.76c Identify the major and minor product(s) of the following reaction: Br i NaOEt Norden ? If there is more than one minor product, be sure to draw all of them. Practice Problem 07.76e Identify the major and minor product(s) of the following reaction: ohan NaOEt...
Question 33 Draw the major and minor product(s) that are expected for the following reaction. If only one product is formed, draw it as the major product, and select no reaction for the minor product. Draw all of the minor products if more than one will form in the following reaction. ? EtOH Heat eGet help answering Molecular Drawing questions Draw the major product: Edit 2Get help answering Molecular Drawing questions Draw the minor product(s): Edit No reaction
Draw the products in the following reaction. Identify which mechanism(s) the reaction will undergo. S_N1 S_N2 E1 E2 The number of E_2 product(s): 2 The E2 products: (major) (minor)
1. Suggest a reasonable mechanism for the following reaction mage. i.EtON, EtOH, 25°C ii. Hz0 Answer: 2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale. Answer:
Predict the elimination products for the following reaction. Identify the major and minor stereoisomers and draw them in the indicated box. This is a possible product, but the two phenyl rings repulse sterically, making this unstable. Consider the other more stable stereoisomer.
1. Suggest a reasonable mechanism for the following reaction. na za i.EtON, EtOH, 25°C ii. H30 Answer: 2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale Answer:
Question 32 Draw the major and minor product(s) that are expected for the following reaction. If only one product is formed, draw it as the major product, and select no reaction for the minor product. Draw all of the minor products if more than one will form in the following reaction. Draw the major product:Draw the minor product(s):Question 31 Draw the major and minor product(s) that are expected for the following reaction. If only one product is formed, draw it as the major...
Predict the major organic product of the following reaction and complete its mechanism below. 1) NaOEt/EtOH 2) CH3CH2CH2Br 3) dilute NaOH/heat 4) H30* 5) heat Complete the curved-arrow mechanism for the scheme below by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows. :O O: :Br. CH3CH2OH Do not show curved arrows for this step. Added acid Dilute HH NaOH and heat hydrolyzes the ester. O: Na Br - H20, Na* O: 100-150 °C O:
1. Suggest a reasonable mechanism for the following reaction. nagogo i.EtON, EtOH, 25°C ii. H,0 Answer: 2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale Answer: