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Hi I have a question 👇👇 Let us assume you move at 90% of the speed of light and observe an apple falling from the tree. Problem : would the apple appear to fall faster or slower compared to what you would have observed if you were just chilling by the side of tree(stationary) Case 1: Since moving closer to the speed of light it should appear to fall slowly according to time dilation (I found on the internet ) Case 2: Since moving closer to the speed of light makes your clock tick slower than the resting clock and you age slower you should experience the world in fast forward making the apple appear dropping faster.( Quite opposite of any movie and series speedster) Which one is true?

Nice Thumbnail...How to make this?

How to make this kind of Thumbnail???😮

Humans do the same think,g, only with money

Who knew, this was going on inside a boiled egg, WOW 🤯 interesting stuff

Helpful

Thank you

Thank you❤

Fischer is a genius and thank you .Your explanation is easy to understand.

Thanks

Only reading isn't enough to make understand someone. You shall make us understand by exaggerating the hidden concept!

Can you please tell me what anomeric effect actually is.?...Plz sir tommorow is my exam and this question holds my 3 marks so please Tell in easy language what is anomeric effect .? ...

This has helped me a lot ,thank you for the video

Thanks a lot 😊

my man out here trying really hard to disguise his ethnnicity.

Thank you

tnq soo much

good one

❤️❤️

This video is very helpful, Thank you so much sir. Due to online classes, we can't understand the topics. But after watching this video, clearly understood.

For anyone interested in 15:00 why the coupling constant is lower for the alpha anomer than for beta. It is because in the beta anomer the hydrogens are both axial (axial-axial), whilst in alpha anomer they are axial-equatorial. The Karplus relationship tells us that axial-axial couplings are larger (180 degree dihedral angle) than 60 dg angle axial-equatorial or eq-eq couplings.

Short and informative. Thanks!!

Can you provide the mechanism of conversion of osazone to osone using benzaldehye in acidic medium?

Thank you!

Baddddd

Where is sound 😑

...so you have the alcohol resonance form of the aldose having its -OH group attack the NO2- anion. Could we have instead, the NO2- anion attacking the carbonyl carbon of the aldehyde resonance form of the aldose?

This copy from Wikipedia

Can you explain me why formation of methyl glucopyranoside can't takes place in basic medium only in acidic medium ?

what is the length of edge for this structure?

Thanks for kind explanation. Superb!

Tnq

Thanks!

Thank you sir

Sir, pls upload detail mechanism pls

Sir give more examples of deoxy sugars.....

How to explain effect on bond length of this effect

U don't sound very sure of wut ur saying... Speak more confidently...

how do you where the sigma star orbital is located?

nice glove

Sir i am very happy to see this lecture.... many problem of carbohydrates i had.. but now all is solved... thanks sir

Nice vid

Good job bro....go ahead..👍