c. condensation is your answer.
They can grow fungus and they emit carbon
CS2 + 3O2 = CO2 + 2SO2
1 mole of CS2 gives 1 mole of CO2
12 + 2(32) = 76g of CS2 yields 44 g of CO2
Theoretically 1 g of CS2 yields 44/76 g CO2
Therefore 50 g CS2 should yield 50*44 / 76 = 28.95 g
So % yield = 103.6 % ( which is not possible because you can't create matter from nothing).
The 30g cannot be right . This is experimental err.
Electronegativity is the strength an atom has to attract a bonding pair of electrons to itself. When a chlorine atom covalently bonds to another chlorine atom, the shared electron pair is shared equally. The electron density that comprises the covalent bond is located halfway between the two atoms.
But what happens when the two atoms involved in a bond aren’t the same? The two positively charged nuclei have different attractive forces; they “pull” on the electron pair to different degrees. The end result is that the electron pair is shifted toward one atom.
ATTRACTING ELECTRONS: ELECTRONEGATIVITIES
The larger the value of the electronegativity, the greater the atom’s strength to attract a bonding pair of electrons. The following figure shows the electronegativity values of the various elements below each element symbol on the periodic table. With a few exceptions, the electronegativities increase, from left to right, in a period, and decrease, from top to bottom, in a family.
Electronegativities give information about what will happen to the bonding pair of electrons when two atoms bond. A bond in which the electron pair is equally shared is called a nonpolar covalent bond. You have a nonpolar covalent bond anytime the two atoms involved in the bond are the same or anytime the difference in the electronegativities of the atoms involved in the bond is very small.

Now consider hydrogen chloride (HCl). Hydrogen has an electronegativity of 2.1, and chlorine has an electronegativity of 3.0. The electron pair that is bonding HCl together shifts toward the chlorine atom because it has a larger electronegativity value.
A bond in which the electron pair is shifted toward one atom is called a polar covalent bond. The atom that more strongly attracts the bonding electron pair is slightly more negative, while the other atom is slightly more positive. The larger the difference in the electronegativities, the more negative and positive the atoms become.
Now look at a case in which the two atoms have extremely different electronegativities — sodium chloride (NaCl). Sodium chloride is ionically bonded. An electron has transferred from sodium to chlorine. Sodium has an electronegativity of 1.0, and chlorine has an electronegativity of 3.0.
That’s an electronegativity difference of 2.0 (3.0 – 1.0), making the bond between the two atoms very, very polar. In fact, the electronegativity difference provides another way of predicting the kind of bond that will form between two elements, as indicated in the following table.
Electronegativity DifferenceType of Bond Formed0.0 to 0.2nonpolar covalent0.3 to 1.4polar covalent> 1.5ionic
The presence of a polar covalent bond in a molecule can
Divide
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.
