Answer:
The balanced molecular equation for the reaction :
Explanation:
The reaction between copper(II) nitrate and potassium carbonate gives solid precipitate of copper(II) carbonate and aqueous solution of potassium nitrate.
According to reaction, 1 mole of copper(II) nitrate reacts with 1 mole of potassium carbonate to give 1 mole of copper(II) carbonate and 2 moles of potassium nitrate,
Answer:
Here's what I get
Explanation:
A plant extract is a mixture because it contains different substances: acetone or ethanol, chlorophylls A and B, carotene and xanthophylls.
It is homogeneous because it is a solution. There is only one phase: the liquid phase. You cannot see the pigments as separate phases.
You can separate the pigments by paper, thin layer, or column chromatography.
Many schools use paper chromatography, because paper is cheap.
As the mixture of pigments follows the solvent up the paper, they separate into different coloured bands according to their attractive forces to the cellulose in the paper.
The chlorophylls are strongly attracted to the paper, so they don't travel very far.
The nonpolar carotene molecules have little attraction to the polar cellulose, so they are carried along by the solvent front.
Answer:
See explanation and picture below
Explanation:
First, in the case of methyloxirane (Also known as propilene oxide) the mechanism that is taking place there is something similar to a Sn2 mechanism. Although a Sn2 mechanism is a bimolecular substitution taking place in only step, the mechanism followed here is pretty similar after the first step.
In both cases, the H atom of the HBr goes to the oxygen in the molecule. You'll have a OH⁺ in both. However, in the case of methyloxirane the next step is a Sn2 mechanism step, the bromide ion will go to the less substitued carbon, because the methyl group is exerting a steric hindrance. Not a big one but it has a little effect there, that's why the bromide will rather go to the carbon with more hydrogens. and the final product is formed.
In the case of phenyloxirane, once the OH⁺ is formed, the next step is a Sn1 mechanism. In this case, the bond C - OH⁺ is opened on the side of the phenyl to stabilize the OH. This is because that carbon is more stable than the carbon with no phenyl. (A 3° carbon is more stable than a 2° carbon). Therefore, when this bond opens, the bromide will go there in the next step, and the final product is formed. See picture below for mechanism and products.
