Predict the major organic product of the given reaction.Step 1: Draw curved arrows.Complete the curved-arrow mechanism for the scheme by adding any missing atoms, bonds, charges, nonbonding electrons, andcurved arrows. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the structure,click the undo button in the lower left.1. NaOEVEIOH2. CH₂CH₂CH₂Br3. dilute NaOH/heatdilute NaOH4. H₂O*5. HeatStep 2: Addition of propyl bromide. Complete the structure and draw curved arrows.and heatStep 3: complete the intermediate. Do not draw curved arrows.hydrolyzesthe ester.:01theStep 4: Hydrolysis of the ester and protonation of the carboxylate salt.EXT-ö: Na*20:70:10:HStep 5: The intermediate is heated. Draw curved arrows.H-O-HH-H₂O, Na+-CH₂CH₂OH100-150 C

While writing the mechanism use electron pushing arrow from electron rich center to electron poor…

edict the major organic product of the given reaction. Step 1: Draw curved arrows. 1. NOEVEIOH 2. CH₂CH₂CH₂Br 3. dute NaOHheat omplete the curved-arrow mechanism for the scheme by adding any missing atoms, bonds, charges, nonbonding electrons, and rved arrows. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the structure, ick the undo button in the lower left. 4. H₂O 5. Heat Step 2: Addition of propyl bromide. Complete the structure and draw curved arrows. llen Step 3: complete the intermediate. Do not draw curved arrows. dilute NaOH and heat hydrolyzes the ester. ep 4: Hydrolysis of the ester and protonation of the carboxylate salt. ext- H -H₂O, Na* Na H-O-H Step 5: The intermediate is heated. Draw curved arrows. 10: -CH₂CH₂OH 100-150 C

edict the major organic product of the given reaction. Step 1: Draw curved arrows. 1. NOEVEIOH 2. CH₂CH₂CH₂Br 3. dute NaOHheat omplete the curved-arrow mechanism for the scheme by adding any missing atoms, bonds, charges, nonbonding electrons, and rved arrows. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the structure, ick the undo button in the lower left. 4. H₂O 5. Heat Step 2: Addition of propyl bromide. Complete the structure and draw curved arrows. llen Step 3: complete the intermediate. Do not draw curved arrows. dilute NaOH and heat hydrolyzes the ester. ep 4: Hydrolysis of the ester and protonation of the carboxylate salt. ext- H -H₂O, Na* Na H-O-H Step 5: The intermediate is heated. Draw curved arrows. 10: -CH₂CH₂OH 100-150 C

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Give typed full explanation not a single word hand written otherwise leave it
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Instructions: a,ß-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as shown below. Use this information to answer the following question(s). + Nu-H Nu H Refer to instructions. Draw a resonance form for the unsaturated carbonyl that accounts for this reactivity.
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