Answer:
They are held together by hydrogen bonds
Explanation:
Hydrogen bonds are special dipole-dipole attractions between polar molecules in which a hydrogen atom is directly joined to a highly electronegative atom(oxygen or nitorgen or fluorine).
Such molecules includes water, alkanoic acids, ammonia and amines.
A hydrogen nucleus has a high concentration of positive charge. The bond is actually an electrostatic attraction between the hydrogen atom of one molecule and the electronegative atom(O or N or F).
Hydrogen bonds are very effective in binding molecules into larger units. Most substances that joins with hydrogen bonds have a higher boiling point and lower volatility.
This is why we have a strong intermolecular bond between water molecules.
The majority of wind turbines consist of three blades mounted to a tower made from tubular steel. There are less common varieties with two blades, or with concrete or steel lattice towers. At 100 feet or more above the ground, the tower allows the turbine to take advantage of faster wind speeds found at higher altitudes.
Turbines catch the wind's energy with their propeller-like blades, which act much like an airplane wing. When the wind blows, a pocket of low-pressure air forms on one side of the blade. The low-pressure air pocket then pulls the blade toward it, causing the rotor to turn. This is called lift. The force of the lift is much stronger than the wind's force against the front side of the blade, which is called drag. The combination of lift and drag causes the rotor to spin like a propeller. So therefore your answer would be A.
If this helped could you leave a brainlyest?
Answer:
Explanation:
In this case we want to know the structures of A (C6H12), B (C6H13Br) and C (C6H14).
A and C reacts with two differents reagents and conditions, however both of them gives the same product.
Let's analyze each reaction.
First, C6H12 has the general formula of an alkene or cycloalkane. However, when we look at the reagents, which are HBr in ROOR, and the final product, we can see that this is an adition reaction where the H and Br were added to a molecule, therefore we can conclude that the initial reactant is an alkene. Now, what happens next? A is reacting with HBr. In general terms when we have an adition of a molecule to a reactant like HBr (Adding electrophyle and nucleophyle) this kind of reactions follows the markonikov's rule that states that the hydrogen will go to the carbon with more hydrogens, and the nucleophyle will go to the carbon with less hydrogen (Atom that can be stabilized with charge). But in this case, we have something else and is the use of the ROOR, this is a peroxide so, instead of follow the markonikov rule, it will do the opposite, the hydrogen to the more substituted carbon and the bromine to the carbon with more hydrogens. This is called the antimarkonikov rule. Picture attached show the possible structure for A. The alkene would have to be the 1-hexene.
Now in the second case we have C, reacting with bromine in light to give also B. C has the formula C6H14 which is the formula for an alkane and once again we are having an adition reaction. In this case, conditions are given to do an adition reaction in an alkane. bromine in presence of light promoves the adition of the bromine to the molecule of alkane. In this case it can go to the carbon with more hydrogen or less hydrogens, but it will prefer the carbon with more hydrogens. In this case would be the terminal hydrogens of the molecules. In this case, it will form product B again. the alkane here would be the hexane. See picture for structures.
The mass of Hydrogen is 2 g/mol
The mass of Helium is 4 g/mol
Answer:
four million two hundred and thirty
Explanation: