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Methyl anion, electrostatic potential

Electrostatic potential map for pyramidal 2-methyl-2-propyl anion shows most negatively-charged regions (in red) and less negatively-charged regions (in blue). [Pg.42]

Compare electrostatic potential maps for planar and pyramidal forms of 2-methyl-2-propyl anion. For which is the negative charge more delocalized Is this the lower-energy structure For this case, does charge delocalization lead to stabilization Explain. [Pg.42]

Examine atomic charges and the electrostatic potential nu for nitrite anion. Which atom(s) is most electron riel Which product would be obtained if this atom behav as a nucleophile in its reation with methyl bromide. [Pg.88]

A comparison of methyl, vinylic, and acetylide anions. The acetylide anion, with sp hybridization, has more s character and is more stable. Electrostatic potential maps show that placing the negative charge closer to a carbon nucleus makes carbon appear less negative (red). [Pg.288]

Use SpartanView to compare electrostatic potential maps of styrene, 2-methyl-propene, 2-propenal, and nitroethylene. Which alkenes look like they would make good substrates for anionic polymerization For cationic polymerization Explain. [Pg.1284]


See other pages where Methyl anion, electrostatic potential is mentioned: [Pg.1306]    [Pg.33]    [Pg.1306]    [Pg.33]    [Pg.482]    [Pg.475]    [Pg.37]    [Pg.105]    [Pg.192]    [Pg.245]    [Pg.51]    [Pg.52]    [Pg.105]    [Pg.666]    [Pg.1132]    [Pg.491]    [Pg.130]    [Pg.137]    [Pg.2426]    [Pg.133]    [Pg.109]    [Pg.62]   


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Methyl anion

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