Alcohol Reactions - HBr, PBr3, SOCl2

[@TheOrganicChemistryTutor]

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[@CHEMISTRYSUPERSTAR]

14:00 please correct.....Alcohol with SOCl2 without pyridine give retention & mechanism is not SN2 but SNi

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At 13.21 you said Br on on the wedge, not the dash, but in the product you drew it on the dash.

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Boronation reaction

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[@medrizzstudy]

What app have you used sir?

[@G00kGandalf]

What happens if you have PBr3 reacted with 1,2-pentanol or pentan-1,2-ol?

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Of organicchemistry

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Hello sir. can you please tell me which software are you using? . for drawing the structures &etc.

[@maheswaraakram2216]

can we replace zncl2 with another catalyst?

[@carrydedier9952]

I think AlCl3 would work too

[@franciskodua6499]

Hello, please am confused when you said PBr3 even though reacting with the secondary alcohol proceeds through an SN2 reaction. Because we know secondary and tertiary alcohols are SN1 reactions.

[@alexandervalchev6725]

They proceed in an sn2 reaction whenever they react with hydrogen halides

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[@beautyyfloweerr3452]

isnt it wrong at 5:38? because this is an sn2 reaction, and sn2 does not have rearrangement????

[@IndigoMist44]

that's what i was thinking; isn't it sn2?

[@Tag_Gw]

Before sn2 reaction

[@Tag_Gw]

Because markovnikov rule i mean we all want to be more stable

[@aryangaming90398]

What about [ Zn(OH) Cl2]

[@yura2424]

11:08 Is there any prove that the reaction actually takes these steps?

[@김강민-n2u]

in 9:05, 1-carbon is bond with H,H,O,C to H,H,Br,C . How can I think this is inversion at carbon?

[@alissaa.2287]

why does PBr3 proceed by Sn2?

[@CHEMISTRYSUPERSTAR]

not actually Sn2 but overall finally inversion is observed .

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[@YouMockMe]

Oh, ok! So the O in Ethanol(?) has a stronger polarity than Br so it takes the H from HBr (to be H2O and Ethylbromide?) Dig it (noob, thanks COVID hahahaha).

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14:25

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Why can't we just attack the OH with Br- and Cl- rather than adding a base?

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No

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Boss Hoffman bromination

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[@varunvarmanadimpalli7968]

10:44 But in the case of socl2 using pyridine as the solvent isn't it going to form a compound that has the socl2 molecule without any chlorines but the alcohol on one side and the pyridine on the other?

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12:25