Answer:
Explanation has been given below.
Explanation:
- Chloroform has three polar C-Cl bonds. Methylene chloride has two polar C-Cl bonds. So it is expected that chloroform should be more polar and posses higher dipole moment than methylene chloride.
- Two factors are liable for the opposite trend observed in dipole moments of methylene chloride and chloroform.
- First one is the number of hyperconjugative hydrogen atoms present in a molecule. Hyperconjugation occurs with vacant d-orbital of Cl atom. Hyperconjugation amplifies charge separation in a molecule resulting higher dipole moment.
- Methylene chloride has two hyperconjugative hydrogen atoms and chloroform has one hyperconjugative hydrogen atom.Therefore methylene chloride should have higher charge separation as compared to chloroform.
- Second one is induction of opposite polarity in a C-Cl bond by another C-Cl bond in a molecule. Higher the opposite induction of polarity, lower the charge separation in a molecule and hence lower the dipole moment of a molecule.
- Chloroform has three C-Cl bonds and methylene chloride has two C-Cl bonds. Therefore opposite induction is higher for chloroform resulting it's lower dipole moment.
1. Make a Prediction
2. Fill both beakers with water
3. Dissolve salt in one of the beakers
4. Place both in the freezer and observe
5. Write a report
(Always make the prediction first! That's a hypothesis!)
5 plates is the highest amount that can be served
There’s only 5 sandwiches so 7 is automatically ruled out, there’s 14 corn cobs and 5 sandwiches only need 10 so it works out
Copper nitrate and nitric oxide are produced in this reaction.
The Lewis structure of
Diimide (N₂H₂) is shown below.
In this molecule two Nitrogen atoms attached to each other through a
double bond are further attached to one one Hydrogen atom. Also, each Nitrogen atom carries one
non-binding electron pair (
Lone Pair) (Highlighted RED).
Result: Option-C (<span>each nitrogen has one nonbinding electron pair) is the correct answer.</span>