a) Identify the alkyl halide (i.e., an alkane chain attached to a halogen) as primary, secondary, or tertiary. b) Draw the carbocation upon spontaneous dissociation between the C and Br atom. c) Identify the carbocation as primary, secondary, or tertiary. d) Is rearrangement possible, if yes, then draw that outcome and label the carbocation type (e.g., primary, secondary, or tertiary etc.). Br Browser Downloads 0 Files Settings

Cl₂ H₂O Draw the curved arrow step in this column... example: 1 H H OH CH3 CH3 + enantiomer CI: this mechanism requires. three mechanistic steps And complete sentence in this column In this mechanistic step, the nucleophilic alkene is attacking the chlorine which can be slightly electrophilic due to Cl₂'s polarizability, however, the extra lone pair on chlorine can attack one of the sp2 C resulting in the cationic complex

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Draw an arrow on the carbocation in the box on the left to show how it rearranges to the carbocation in the box on the right. 1st attempt See Periodic Add the missing curved arrow notation. ®, + 3 OF 25 QUESTIONS COMPLETED

Need to check answer 1.Borane (BH3) adds to alkenes to form an alkylborane. In the first box draw the mechanism arrows, and in the second box draw the correct product. Be sure to add lone pairs of electrons and nonzero formal charges to all species.

Please correct answer and don't use hend raiting

draw the missing resonance structure

Select the set of curved arrows that best illustrates electron movement in a reaction. ||| :Br :Br: :CI: CI: IV :Br: :Br:

[References] Follow the flow of electrons indicated by the curved arrows in the following polar reaction. Draw all products that result, including any inorganic ions. H H₂O CH3 H3C • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Include all valence lone pairs in your answer. ? ChemDoodle F Previous Next