Amino Acids undergo a kind of acid base reaction within a molecule. The
Amino group acts as a base and accepts proton from
Carboxylic functional group resulting in formation of
Ammonium with positive charge and a negative charge on
Carboxylate. Such molecules containing both positive and negative charges are called as
Zwittor Ions.
Phenylalanine both in Un-ionized and Ionized form is shown below,
As we know,
1 D = 3.34 × 10⁻³⁰ C.m
So,
1.44 D = ?
Solving for 1.44 D,
= (3.34 × 10⁻³⁰ C.m × 1.44 D) ÷ 1 D
1.44 D = 4.80 × 10⁻³⁰ C.m
Dipole Moment is given as,
Dipole Moment = q × r
Solving for q,
q = Dipole Moment / r ------ (1)
Where,
Dipole Moment = 4.80 × 10⁻³⁰ C.m
r = 163 pm = 1.63 × 10⁻¹⁰ m
Putting values in eq. 1,
q = 4.80 × 10⁻³⁰ C.m / 1.63 × 10⁻¹⁰ m
q = 2.94 × 10⁻²⁰ C
As,
1.602 × 10⁻¹⁹ C = 1 e⁻
So,
2.94 × 10⁻²⁰ C = X e⁻
Solving for X,
X = (2.94 × 10⁻²⁰ C × 1 e⁻) ÷ 1.602 × 10⁻¹⁹ C
= 0.183 e⁻
Result:
So one element is containing + 0.183 e⁻ while the other element is containing - 0.183 e⁻.
I think that it is shear adhesion
Answer:
Mostly Para
Explanation:
First, let's assume that the molecule is the toluene (A benzene with a methyl group as radical).
Now the nitration reaction is a reaction in which the nitric acid in presence of sulfuric acid, react with the benzene molecule, to introduce the nitro group into the molecule. The nitro group is a relative strong deactiviting group and is metha director, so, further reactions that occur will be in the metha position.
Now, in this case, the methyl group is a weak activating group in the molecule of benzene, and is always ortho and para director for the simple fact that this molecule (The methyl group) is a donor of electrons instead of atracting group of electrons. Therefore for these two reasons, when the nitration occurs,it will go to the ortho or para position.
Now which position will prefer to go? it's true it can go either ortho or para, however, let's use the steric hindrance principle. Although the methyl group it's not a very voluminous and big molecule, it still exerts a little steric hindrance, and the nitro group would rather go to a position where no molecule is present so it can attach easily. It's like you have two doors that lead to the same place, but in one door you have a kid in the middle and the other door is free to go, you'll rather pass by the door which is free instead of the door with the kid in the middle even though you can pass for that door too. Same thing happens here. Therefore the correct option will be mostly para.
