Answer a):-
Mechanism:-
The mechanism involves the nucleophilic attack of propyl carboanion from grignard reagent to carbonyl carbon , producing an alkoxide intermediate. Thus is followed by acidic workup, to form alcohol as major product.
----------------
Answer b):-
Mechanism:-
The mechanism involves attack of hydride ion to the carbonyl carbon to form alkoxide ion. This is followed by protonation to form an alcohol as a major product.
provide the major organic products and draw out detailed mechanism with electron pushing arrows. 1. CH...
1. Advanced Electron Pushing!! Provide a detailed, stepwise mechanism for the following transformations. Use curved arrows to show the movement of electrons. Ph NaOMe lelic:01 1 OMe
a) complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. a) Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the Draw the structure of the organic product formed in the reaction. Draw lone pairs. conversion to the product. CH3CH2OH -CI...
1) Provide a detailed electron pushing mechanism for the below transformation. Show ALL relevant resonance structures to help explain why the para product is the major organic product. (Note: your electron pushing mechanism should include formation of the electrophile) (4 points) Cl AICl3
Organic Chemistry 2 Please show detailed arrow-pushing mechanism. Best regards. B) Predict the products for the reactions below (2 points per box, 4 points total section). MgBr SH Major product Major product
a) Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. CH3 :Ci: CH3CH2OH -Cl b) Select the option that describes the mechanism of the reaction above. O E1 O E2
Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. Select the option that describes the mechanism of the reaction above. S_N1 S_N2 E1 E2
Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. Select the option that describes the mechanism of the reaction above. S_N1 S_N2 E1 E2
Provide the electron-pushing arrows to complete the mechanism below. Identify the arrow-pushing pattern(s) used in each step. (1) Provide electron-pushing arrows to complete the mechanism shown below. Identify the arrow.pushing pattern(s) used at each step. :NH3 H H-NH2 -NH2 NO RO: R R 0 I- -H20 NH2 .NH HN R
Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. 1. Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. (6 pts) 2 OH H2O HCI
please draw the full mechanism with all electron pushing arrows, reactant structures, intermediates, and products for the hydroboration oxidation reaction using 1-octene to prepare 1-octanol.