WILL GIVE BRANLIEST!! EASY BUT I WAS TO LAZY TO LEARN!! WILL FOREVER BE GREATFUL!!! WILL GIVE BRANLIEST!! EASY BUT I WAS TO LAZY
1 answer:
You might be interested in
Answer:
The range of atoms = (30-300 pm) depending upon the element
Explanation:
The Atomic radii of the atom is the distance from the center of the circle to the outermost orbital.
The center of the circle is the nucleus and the radii is the outermost boundary.
The actual size of the atom is decided on the basis of the Zeff . Also known as <em>effective nuclear charge.</em>
<em>Zeff: It is the net positive charge felt by the outermost electron by the nucleus.</em>
<em>The value of Zeff depends upon the shielding constant. More the shielding less will be the Zeff . Hence the size of the atom increases.</em>
Due to shielding the outermost electrons feel less pull of nucleus.
<em>The greater the Zeff , the smaller the radius of the atom.</em>
The formula used to calculate the atomic mass is :
pm
Here "pm"= picometers
<u>The size of the smallest atom H-atom = 120 pm</u>
<u>The range of atoms = (30-300 pm)</u>
Answer:
Here's what I get
Explanation:
You may have done a Williamson synthesis of guaifenesin by reacting guaiacol with 3-chloropropane-1,2-diol.
A. Mechanism
Step 1
NaOH converts guaiacol into a phenoxide ion.
Step 2
The phenoxide acts as the nucleophile in an SN2 reaction to displace the Cl from the alkyl halide.
B. Improve the yield
You probably carried out the reaction in ethanol solution — a polar protic solvent.
You might try doing the reaction in a polar aprotic solvent— perhaps DMSO.
A polar aprotic solvent does not hydrogen bond to nucleophiles, so they become stronger.
C. Another method of ether synthesis —dehydration of alcohols
Sulfuric acid catalyzes the conversion of primary alcohols to ethers.
This is also a nucleophilic displacement reaction.
Protonation of the OH converts it into a better leaving group.
Attack by a second molecule of alcohol forms the protonated ether.
A molecule of water then removes the proton.
