There are 2 peaks are in the proton spin decoupled 13C NMR spectrum of 1,3,5-trinitrobenzene .
The 13C NMR spectrum give the peak which is directly about the carbon skeleton not just the proton attached to it . The number of signals tell us how many different carbons or set of equivalent carbons . The splitting of a signal tells us how many hydrogens are attached to each carbon.
In 1,3,5-trinitrobenzene molecule , there are 2 peaks are in the proton spin decoupled 13C NMR spectrum three carbon give one signal and another three carbon give another one signal .
To learn more about NMR spectrum
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The correct reference for this isotope is A. Oxygen-18.
Answer: The Lewis structure of Chloroacetate can be found at the attachment below.
Explanation:
CH2ClCOO- The chemical compound is called Chloroacetate.
Reference link for the Chloroacetate structure.
https://www.google.com/search?q=lewis+structure+for+CH2ClCOO-&prmd=ivn&sxsrf=ALeKk03mQcLiY-q5pEriMR0_26ZTXLjmJg:1589680325594&source=lnms&tbm=isch&sa=X&ved=2ahUKEwjfxPPY5LnpAhVloXEKHeAwD-wQ_AUoAXoECA4QAQ&cshid=1589680746615&biw=360&bih=559&dpr=3#
Explanation:
gravity if it's incorrect sorry
