What type(s) of intermolecular forces are expected between ch3ch2ch2ch2ch2oh molecules?
1 answer:
Answer : Hydrogen-bonding, Dipole-dipole attraction and London-dispersion force.
Explanation :
The given molecule is,
Three types of inter-molecular forces are present in this molecule which are Hydrogen-bonding, Dipole-dipole attraction and London-dispersion force.
- Hydrogen-bonding : when the partial positive end of hydrogen is bonded with the partial negative end of another molecule like, oxygen, nitrogen, etc.
- Dipole-dipole attraction : When the partial positively charged part of the molecule is interact with the partial negatively charged part of the molecule. For example : In case of HCl.
- London-dispersion force : This force is present in all type of molecule whether it is a polar or non-polar, ionic or covalent. For example : In case of Br-Br , F-F, etc
Hydrogen-bonding is present between the oxygen and hydrogen molecule.
Dipole-dipole forces is present between the carbon and oxygen molecule.
London-dispersion forces is present between the carbon and carbon molecule.
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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#
Answer:
<h2>1.9</h2>Explanation:
The pH of a solution can be found by using the formula
From the question we have
We have the final answer as
<h3>1.9</h3>Hope this helps you
Answer:
Here's what I get
Explanation:
(a) Intermediates
The three structures below represent one contributor to the resonance-stabilized intermediate, in which the lone pair electrons on the heteroatom are participating (the + charge on the heteroatoms do not show up very well).
(b) Relative Stabilities
The relative stabilities decrease in the order shown.
N is more basic than O, so NH₂ is the best electron donating group (EDG) and will best stabilize the positive charge in the ring. However, the lone pair electrons on the N in acetanilide are also involved in resonance with the carbonyl group, so they are not as available for stabilization of the ring.
(c) Relative reactivities
The relative reactivities would be
C₆H₅-NH₂ > C₆H₅-OCH₃ > C₆H₅-NHCOCH₃
