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Learning i'm pronouncing a word wrong does not change the way I pronounce a word. It only changes how I pronounce it in front of other people, like, mine sounds better don't know what to tell you
ํํ์์ฌ, ์์ฝํ, ํ๋ผ์คํฑ ๋ฑ ์ฐ๋ฆฌ๊ฐ ์๋นํ๋ ๋๋ถ๋ถ์ ๊ณต์ฐํ์ ์ ๊ธฐํํ ๋ฐ์์ ์ฐ๋ฌผ์ด๋ค. A๋ผ๋ ๋ฌผ์ง์ด ํํ๋ฐ์์ ๊ฑฐ์ณ B๋ผ๋ ๋ฌผ์ง๋ก ๋ณํ ๋ ์งง์ ์๋ช ์ ๊ฐ์ง ์ค๊ฐ๋จ๊ณ๋ฅผ ๊ฑฐ์น๋๋ฐ, ์ด ์ค๊ฐ๋ฌผ์ง์ ํ๋๊ฐ โํ์์์ด์จโ์ด๋ค.* ํ์์์ด์จ(Carbocation) : ์์ ํ๋ฅผ ๋ค ํ์ ์โฆ
The fact that atoms that we normally think of as electron-wthdrawing (nitrogen, oxygen, chlorine) can actually be electron-donor groups is probably one of the most difficult factors to wrap your head around in Org 2.
James Ashenhurst, Three Things That Stabilize Carbocations
im having trouble in understanding carbocation reaction ๐ญ

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ELECTROPHILIC ADDITION OF ALKENES
One day an alkene was just trollollolling along, minding his own business, as alkenes do. What he didn't realise that the double bond C=C he posessed in his stomach, was actually a really HIGH AREA OF ELECTRON DENSITY :o
An area that ELECTROPHILES are attracted to. An electrophile is an electron-deficent species that takes part in an organic reaction by attacking areas of high electron density in another reactant. :o An example of an electrophile is HBr, hydrogen bromide.ย
This electrophile was all alone. He only had a partially positively charged area. All he wanted was some company from some fellow electrons. He couldn't help but be attracted to the double bond in the alkene.
Fortunately, the alkene couldย sympathize with the electrophile.ย ย The electrophile accepted a pair of electrons kindly donated by the double bond in the alkene.
The alkene had been hoping for change, some transformation. He was bored of the alkene life. He wanted to be free. He wanted to grow up to be a haloalkane ever since he was little boy.
In order for this to happen, a positive ion a CARBOCATION forms. A negatively charged ion (in this case Bromide) and forms a bond with the carbocation.
And everyone lives happily ever after.