So that you can learn while being safe. Wearing goggles, for eye protection when dealing with chemicals
Its air and water. if its multiple choice
Explanation:
Distinguish chemical substances from mixtures
Key Points
Matter can be broken down into two categories: pure substances and mixtures. Pure substances are further broken down into elements and compounds. Mixtures are physically combined structures that can be separated into their original components.
A chemical substance is composed of one type of atom or molecule.
A mixture is composed of different types of atoms or molecules that are not chemically bonded.
A heterogeneous mixture is a mixture of two or more chemical substances where the various components can be visually distinguished.
A homogeneous mixture is a type of mixture in which the composition is uniform and every part of the solution has the same properties.
Various separation techniques exist in order to separate matter, including include distillation, filtration, evaporation and chromatography. Matter can be in the same phase or in two different phases for this separation to take place.
Terms
substanceA form of matter that has constant chemical composition and characteristic properties. It is composed of one type of atom or molecule.
elementA chemical substance that is made up of a particular kind of atom and cannot be broken down or transformed by a chemical reaction.
mixtureSomething that consists of diverse, non-bonded elements or molecules.
Na = 23 x 2.40 = 55.2
O = 16 x 2.40 = 38.4
H = 1 x 2.40 = 2.40
55.2 + 38.4 + 2.4 = 96
2.40 mol of NaOH = 96 amu
Answer:
See explanation
Explanation:
The reaction that we are considering here is quite a knotty reaction. It is difficult to decide if the mechanism is actually E1 or E2 since both are equally probable based on the mass of scientific evidence regarding this reaction. However, we can easily assume that the methylenecyclohexane was formed by an E1 mechanism.
Looking at the products, one could convincingly assert that the reaction leading to the formation of the two main products proceeds via an E1 mechanism with the formation of a carbocation intermediate as has been shown in mechanism attached to this answer. Possible rearrangement of the carbocation yields the 3-methylcyclohexene product.
