The answer is 14.22 mg / (mm^2)
The tert-butyl chloride in ethanol would surely react faster than the solvolysis of 1-chloro-2,2-dimethyl propane. It is known that both reactions are under the SN2 category so it would be hard for these reactions to occur. However, SN1 reactions are possible because of the ethanol which is a polar solvent. Both would form carbocations but tert-butyl chloride forms a more stable carbocation while the 1-chloro-2,2-dimethyl propane forms a primary carbocation only.
Answer:
The predominant intermolecular force in the liquid state of each of these compounds:
ammonia (NH3)
methane (CH4)
and nitrogen trifluoride (NF3)
Explanation:
The types of intermolecular forces:
1.Hydrogen bonding: It is a weak electrostatic force of attraction that exists between the hydrogen atom and a highly electronegative atom like N,O,F.
2.Dipole-dipole interactions: They exist between the oppositely charged dipoles in a polar covalent molecule.
3. London dispersion forces exist between all the atoms and molecules.
NH3 ammonia consists of intermolecular H-bonding.
Methane has London dispersion forces.
Because both carbon and hydrogen has almost similar electronegativity values.
NF3 has dipole-dipole interactions due to the electronegativity variations between nitrogen and fluorine.
An intensive property does not change when you take change when you take away some of the sample the producers that a student could use to examine the intensive property of a rectangular block of wood
Should be :
Lead Sulfate Tetrahydrate
