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iTeachChem

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Reduction

Why will they form different products and also how? Is it cuz of their strength of something to mech?
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redox rxn

its not making sense to me
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Isomerism doubt

How to solve the first ques what should be the thought process got even more confused so made a separate doubt post. Please if someone can provide a detailed solution
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Binomial

Shouldnt it be both c and b? Q55
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Similar ends

Does this structure have similar or dissimilar ends?
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+R -I of benzene

Um... it's kinda troubling to me that if we say overall effect of benzene is -I then how's benzenoic acid less acidic than formic acid... Additionally I even saw that we can just find conjugate like in benzoic acid coo- forms and coo- starts to give +I which is balanced in it but the same ain't even balanced in formic acid so shouldn't it be less acidic??...

pBR322

I know not like many people are there but does anyone like understand what happened in the second step?
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wave optics 3

u = -15cm . f= 10cm so v = 30cm m = -2 the separation b/w two images must be 3mm. a classical YDSE setup can be seen deltax = dx/D = 3lambda ...
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wave optics 2

what will be the path difference
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GOC acidity doubt

NO2 has more -I effect than COOH so why 4th one is more acidic than 1st
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wave optics

how do i get separation b/w two imgs
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Aleternating Current

i feel like the question is incomplete??
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Hemiacetals

Can someone explain the mechanism of addition of alcohol to aldehyde and ketone to prepare acetals and hemiacetals
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Pseudo chiral definition?

In this compound the number of pseudo chiral centres is ?
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