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Problems in Chemistry
United States
เข้าร่วมเมื่อ 22 มี.ค. 2020
This Channel is for anyone who is a science lover - especially chemistry. Alongside I also narrate some of my real life experiences in chemistry.
วีดีโอ
VSEPR Formation of single, double and triple bonds
มุมมอง 19หลายเดือนก่อน
VSEPR Formation of single, double and triple bonds
Strucure of an atom and electron distribution
มุมมอง 6หลายเดือนก่อน
Strucure of an atom and electron distribution
Propose structural formula of C6H13NO
มุมมอง 8510 หลายเดือนก่อน
Propose structural formula of C6H13NO
Predict whether oxidation or reduction
มุมมอง 10411 หลายเดือนก่อน
Predict whether oxidation or reduction
Compound M with molecular formula C5H10O decolorizes Bromine in CCl4
มุมมอง 6911 หลายเดือนก่อน
Compound M with molecular formula C5H10O decolorizes Bromine in CCl4
Compound A with molecular formula C4H9Cl
มุมมอง 10411 หลายเดือนก่อน
Compound A with molecular formula C4H9Cl
Which of these species can be identified by mass spectrometry?
มุมมอง 12611 หลายเดือนก่อน
Which of these species can be identified by mass spectrometry?
Mass Spectrometry Part 10 - Rule of 13
มุมมอง 62611 หลายเดือนก่อน
Mass Spectrometry Part 10 - Rule of 13
Amines Part 10 - Electrophilic Aromatic Substitution Reactions in 5-membered heterocyclic compounds
มุมมอง 677ปีที่แล้ว
Amines Part 10 - Electrophilic Aromatic Substitution Reactions in 5-membered heterocyclic compounds
Amines Part 5 - Electrophilic Aromatic Substitution Reactions in five membered heterocycles
มุมมอง 312ปีที่แล้ว
Amines Part 5 - Electrophilic Aromatic Substitution Reactions in five membered heterocycles
Amines Part 9 - Side chain reactions, diazotization & acidity of methyl group @ C2 & C4 of pyridine
มุมมอง 243ปีที่แล้ว
Amines Part 9 - Side chain reactions, diazotization & acidity of methyl group @ C2 & C4 of pyridine
Amines Part 8 - Nucleophilic Aromatic Substitution of Pyridine
มุมมอง 688ปีที่แล้ว
Amines Part 8 - Nucleophilic Aromatic Substitution of Pyridine
Amines Part 3 - Nomenclature of saturated heterocyclic amines
มุมมอง 225ปีที่แล้ว
Amines Part 3 - Nomenclature of saturated heterocyclic amines
Reactions of Benzene Part 1 - Electrophilic Aromatic Substitution of Benzene - Introduction
มุมมอง 178ปีที่แล้ว
Reactions of Benzene Part 1 - Electrophilic Aromatic Substitution of Benzene - Introduction
Reactions of Benzene Part 9 - Effect of substituents on the pKa of compounds
มุมมอง 445ปีที่แล้ว
Reactions of Benzene Part 9 - Effect of substituents on the pKa of compounds
Benzene and Aromaticity Part 2 - Classifying compounds as aromatic, non- aromatic anti-aromatic
มุมมอง 231ปีที่แล้ว
Benzene and Aromaticity Part 2 - Classifying compounds as aromatic, non- aromatic anti-aromatic
Regioselectivity and Stereoselectivity in Diels Alder Reactions
มุมมอง 458ปีที่แล้ว
Regioselectivity and Stereoselectivity in Diels Alder Reactions
thx alot.
Lovely explanation😊 Indian
Can we rotate in any way ?
Good explanation 😊
Thank you very much, this is the exact explanation I was looking for!!
❤❤
Sir I have a question Do peracids react with alkynes? If it does then what is the product
why vinyl cation is unstable
good question.... The vinyl carbocation is sp hybridized and it is more electronegative than the sp2 hybridized alkyl carbocation Therefore it can't hold the positive charge well. This is more like trying to put a positive charge on an electronegative atom like oxygen in the lewis dot structure. hope this makes sense.
How we know about the peaks?like what kind of this peaks is? like how we know about the intensity of peak?
From it's length
From its height.. the relative abundance
Well Explained...Thanks from India
Good 👍
Ur accent is annoying ...the video was helpful though
❤❤❤pretty easy to understand
V good explanation
Amazing
Thank you so much.!Because of your explanation I have understood this.
Thank you so much 🤍
Man can tell me reference book for this topic
I use 7th edition Bruice's Organic Chemistry. www.amazon.com/Organic-Chemistry-Paula-Yurkanis-Bruice/dp/0321803221
Thank you ❤
Thanks for sharing this amazing video,new friend here 💚
Why wouldn't the sulfuric acid also protonate the alcohol? Such a protonated alcohol would no longer be as good nucleophile as an unprotonated one.
Yes, sulfuric acid can definitely protonate the alcohol but the protonated alcohol is a strong acid with a pKa of -2.5 and therefore gets deprotonated soon. I hope this makes sense.
00:16 Why is this not considered to be an acid-base reaction, if the π bond is clearly acting as a base, grabbing a proton from the hydrogen bromide (which is an acid after all, and a very strong one!), leaving behind its conjugate base - the bromide anion?
Very Helpful
thanks for the explanation
p̳r̳o̳m̳o̳s̳m̳
Just supporting
I think there is a small mistake, for carbon 13, in converting from Hz to MHz, it would be 750 MHz not 75 because you need to move the decimal place twice going from 10^8 to 10^6.
Hi Ellie ,, I said this in class that the gyromagnetic ratio should be changed to 10 power 7.
I knew I was missing one a video ! awesome thanks Dr. V the book didnt do the justice this time appreciate ya
Thanks Angel