It allows people in different places and different countries to use the same units, avoid mistakes and understand each other more easily. The common base 10 of all units makes it easier and has more accurate calculations that are made without cumbersome conversion factors.
Answer:
The answer would be stress
Explanation:
A force that acts on rock to change its shape or volume is stress. Stress adds energy to the rock. The energy is stored in the rock until it changes shape or breaks. Three different kinds of stress can occur in the crust—tension, compression, and shearing.
I hope this helps
The formation of Fossil Fuels.
The fossil fuels such as oil originate mostly from aquatic organism and are extracted on oil rigs located in oceans and seas. Most of the oil is procured this way.
Answer:
No.of moles of C is , n = mass/molar mass = 75.46 g / 12 (g/mol) = 6.3 moles No.of moles of H is , n' = mass/molar mass = 4.43 g / 1.0(g/mol) = 4.43 moles No.of moles of O is , n'' = mass/molar mass = 20.10 g / 16(g/mol) =1.25 moles Ratio to the no.of moles of C,H& O is 6.3 : 4.43 : 1.25 In the simple integer ratio is ( 6.3/1.25) : ( 4.43/1.25) : (1.25/1.25) 5.04 :3.5 : 1
Explanation:
Answer:
See explanation below
Explanation:
The question is incomplete, cause you are not providing the structure. However, I found the question and it's attached in picture 1.
Now, according to this reaction and the product given, we can see that we have sustitution reaction. In the absence of sodium methoxide, the reaction it's no longer in basic medium, so the sustitution reaction that it's promoted here it's not an Sn2 reaction as part a), but instead a Sn1 reaction, and in this we can have the presence of carbocation. What happen here then?, well, the bromine leaves the molecule leaving a secondary carbocation there, but the neighbour carbon (The one in the cycle) has a more stable carbocation, so one atom of hydrogen from that carbon migrates to the carbon with the carbocation to stabilize that carbon, and the result is a tertiary carbocation. When this happens, the methanol can easily go there and form the product.
For question 6a, as it was stated before, the mechanism in that reaction is a Sn2, however, we can have conditions for an E2 reaction and form an alkene. This can be done, cause the extoxide can substract the atoms of hydrogens from either the carbon of the cycle or the terminal methyl of the molecule and will form two different products of elimination. The product formed in greater quantities will be the one where the negative charge is more stable, in this case, in the primary carbon of the methyl it's more stable there, so product 1 will be formed more (See picture 2)
For question 6b, same principle of 6a, when the hydrogen migrates to the 2nd carbocation to form a tertiary carbocation the methanol will promove an E1 reaction with the vecinal carbons and form two eliminations products. See picture 2 for mechanism of reaction.