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.
This is because their tails are hydrophobic and their heads are hydrophilic. Hydrophobic meaning dislikes being near water and hydrophilic meaning likes to be near water. Therefore, they will orientate themselves in such a manner that the heads are facing externally and all the tails are facing together protected by the hydrophilic heads. google a photo of lipid chains in water if you are still confused. I'm not sure if that is what you are asking, but I hope it helps.
Active is more active which means it's in person
Answer:
7 orbitals
Explanation:
An f sublevel has 7 orbitals
UV rays, gamma rays, and x rays
Hope this help