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.
Answer:
in both nucleophil attach the c and leaving group leave but in acyl nu. subsituation c of carbonyl because of double bond with o have bigger positive charge and is better electrophil so do it faster,also alkyl nu. subsituation can have rearangment if going from sn1 and in sn2 sterichemistry of molecule change , acyl nu. subsituation most of time is better
Answer:
Oxidation
Explanation:
Mg loses 2e- for it to gain it's stability hence the reaction above is oxidation
note: Oxidation is the loss of electrons while reduction is the gain of electrons
I believe the anwser is C
I hope this is right! <3
