Mass number<span> is the </span>number<span> of protons </span>and<span> neutrons in an atom.
</span>Atomic mass<span> is the average </span>mass<span> of all the isotopes of a certain type.</span>
Stereochemistry, a subdiscipline of chemistry, involves the study of the relative spatial arrangement of atoms that form the structure of molecules and their manipulation.
<h3>What is the use of stereochemistry?</h3>
Using stereochemistry, chemists can work out the relationships between different molecules that are made up from the same atoms. They can also study the effect on the physical or biological properties these relationships give molecules.
<h3>Why is it called stereochemistry?</h3>
The term “stereochemistry” is derived from the Greek “stereos” meaning solid—it refers to chemistry in three dimensions. Since nearly all organic molecules are three dimensional (with the exception of some olefins and aromatics to be discussed later), stereochemistry cannot be considered a branch of chemistry.
Learn more about stereochemistry here:
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brainly.com/question/13266152</h3><h3 /><h3>#SPJ4</h3>
A garduated cylander, in order to find the amount of water displaced you see how much the water has risen
Answer:
0.897 J/g.⁰C
Explanation:
Given the following data:
m = 170 g (mass)
ΔT = 20.0⁰C (change in temperature)
q = 3050 J (amount of heat)
The amount of heat (q) is calculated as follows:
q = m x Cp x ΔT
Thus, we introduce the data in the mathematical expression to calculate the specific heat (Cp):
Cp = q/(m x ΔT) = 3050 J/(170 g x 20.0⁰C) = 0.897 J/g.⁰C
Answer:
I expect to observe a change in colour from reddish brown to a colourless solution
Explanation:
Bromine (Br2) attacks the electron rich carbon-carbon triple bond in but-2-yne, an alkyne to form an initial product 2, 3 dibromobut-2-ene; which reacts with excess bromine to form a final product 2,2,3,3 -tetrabromobutane.
The reaction occurs in two steps. On approaching but-2-yne, bromine molecule becomes polarised forming an induced dipole containing a bromonium ion.
Br - Br → Br+ - Br-
The bromonium ion (Br+) formed then attacks the carbon - carbon triple bond to form the initial product
2,3- dibromobut-2-ene
CH2-C≡C-CH2 + Br+ →
CH2 - CBr =CBr-CH2
(2,3- dibromobut-2-ene)
Which in the presence of excess bromine gives the final product
2,2,3,3 - tetrabromobutane.
CH2 - CBr =CBr-CH2 + Br2 →
CH3 -CBr2-CBr2 - CH3
2,2,3,3 - tetrabromobutane.
A visible change in colour from the reddish-brown colour of Bromine to a colourless solution is observed during the reaction.