Answer:
D: Carbon
Explanation:
The periodic table lists all the known elements. When looking at it, the only choice you will find is carbon. Therefore, carbon is the element.
Carbon is also by itself, just C.
Water is H2O, which is a molecule due to the 2 different elements.
Carbon Dioxide is CO2, which is a molecule due to the 2 different elements.
Air is just a mixture of different gas molecules, so therefore it is not an element.
The sun heats up the air at different rates. Weather is caused by uneven heating
Answer:
99.24%.
Explanation:
- NaCl reacted with AgNO₃ as in the balanced equation:
<em>NaCl + AgNO₃ → AgCl(↓) + NaNO₃,</em>
1.0 mol of NaCl reacts with 1.0 mol of AgNO₃ to produce 1.0 mol of AgCl and 1.0 mol of NaNO₃.
- We need to calculate the no. of moles of AgCl produced:
no. of moles of AgCl = mass/molar mass = (2.044 g)/(143.32 g/mol) = 0.0143 mol.
- Now, we can calculate the no. of moles of NaCl that can precipitated as AgCl (0.0143 mol), these moles represents the no. of moles of pure NaCl in the sample:
<em>using cross multiplication:</em>
1.0 mol of NaCl produce → 1.0 mol of AgCl, from the stichiometry.
∴ 0.0143 mol of NaCl produce → 0.0143 mol of AgCl.
- Now, we can get the mass of puree NaCl in the sample:
mass of pure NaCl = (no. of moles of pure NaCl)(molar mass of NaCl) = (0.0143 mol)(58.44 g/mol) = 0.8357 g.
∴ The percentage of NaCl in the impure sample = [(mass of pure NaCl)/(mass of the impure sample)] x 100 = [(0.8357 g)/(0.8421 g)] x 100 = 99.24%.
Answer:
1. The product has a higher Rf value on a silica gel TLC plate because it is more polar than the starting methyl benzoate.
2. False
3. True
Explanation:
In chromatography, there is a stationary phase and a mobile phase. The ratio of the distance moved by a component and the distance moved by the solvent gives the retention factor (Rf).
Since silica gel is a polar solvent, it will retain the more polar product methyl m-nitrobenzoate compared to the methyl benzoate starting material.
In comparing the electrophillic aromatic substitution of m-nitrobenzoate and methyl benzoate, we must remember that the presence of electron withdrawing groups (such as -NO2 and -CHO) on the aromatic compound deactivates the compound towards electrophillic aromatic substitution hence, methyl m-nitrobenzoate is less reactive than methyl benzoate in Electrophilic Aromatic Substition and Methyl benzoate is less reactive than benzene in Electrophilic Aromatic Substition