In The carbonyl bond ( CO ), the Carbon attached to O group is electrophilic in nature as the O atom has attracted the electrons towards itself due to electronegativity of O.
In first step, Nucleophile N3 - will attack the electrohilic C , which leads to the resonance of the electron Pair between C and O group.
In step 2, the lone pair of O will attack back and hence , removal of Cl- which is a good leaving group will take place.
Thus, the sequence of steps is
Nucleophilic attack, loss of leaving group.
Do You Remember? Question 2 Which sequence of arrow-pushing patterns matches the events in the following...
Review of Skills - Skill Builder 06.03 Identify each of the four types of arrow pushing patterns. Br :Br: c Rearrangement Proton transfer Loss of leaving group Nucleophilic attack C Proton transfer c Loss of leaving group C Nucleophilic attack c Rearrangement H' "H c Loss of leaving group c Proton transfer c Rearrangement C Nucleophilic attack HsC CH3
In-Class Arrow Pushing Activity Provide the appropriate arrow pushing for the following reactions and identify the arrow- pushing pattern(s) utilized as either loss of a leaving group, nucleophilic attack, proton transfer, or rearrangement. А : NH3 CH, :Br: H2O: :OH (4 steps)
1. For each of the following reactions, identify the arrow-pushing pattern being identified. Pick from nucleophilic attack, leaving group loss, proton transfer, or rearrangement. b oiling orica choch
5. For the following reaction step, indicate which pattern of arrow pushing it represents. Circle one. -Ogr Br A. proton transfer C. nucleophilic attack B. loss of leaving group D. rearrangement 6. The following reaction has three mechanistic steps (down, across, and up). Draw all of the curved arrows necessary to complete the mechanism. (Hint: there should be 4 arrows total.) HBO OH Br H-Br OH2 + H₂ö:
Identify the arrow pushing mechanism shown. o A loss of a leaving group proton transfer O C nucleophilic addition (also called nucleophilic attack) OD methyl shift O E hydride shift
1) Draw the arrows to show bond formation and breaking for the following mechanisms and complete questions b, c, and d. Marking scheme is also provided. (9 marks total) a) All tails of arrows must start at electrons. The arrows must start in the middle of a sigma bond or at a lone pair (2 marks) Take % mark for each mistake until you reach zero. All heads of arrows must end at an atom. (2 marks) Take X mark...
For the following mechanism, identify the sequence of arrow-pushing patterns:
Ohio Inter Homepage- Brigh... g C.. 3. For the following reactions label which ones are a. Nucleophilic Attack, b. Loss of a Leaving Group, c. Proton Transfer (Acid/Base), and d. Rearrangements. For each reaction use arrow pushing to show the mechanism of the reaction and label the nucleophile and electrophile for the reactions exemplifying nucleophilic attack. (4) но + OH Classification CI + CI Classification Н-о Classification Classification 3 Ф O
Fill in the appropriate curved mechanism arrows, missing structures, and/or labels for the following reaction. Labels will either be proton transfer, nucleophilic attack, loss of leaving group, and carbonation rearrangement. .ni 1- nucleophilic attack + OH o OH
Uldwid115 wers diedlcepluie, uut leme Msl vel pur TUISB N we 1. For each of the following reactions, identify the arrow-pushing pattern being identified. Pick from nucleophilic attack leaving group loss, proton transfer, or rearrangement. - i . veria