Give the structure of the product obtained when cyclopropene loses a proton. Will the product be aromatic or not?
1 answer:
Answer:
not aromatic
Explanation:
Cyclopropene -
as the compound is is made to lose a proton , and gains a negative charge on its ring ,
Now, The ring can become aromatic or anti - aromatic depending on the number of π electrobns ,
According to Huckel 's rule ,
The cyclic compounds with ( 4n+2 ) π electrons , where , n = 0, 1, 2, 3 ... , are considered to be aromatic in nature ,
And the cyclic compounds with ( 4n ) π electrons , where , n = 1, 2, 3 ... , are considered to be anti - aromatic in nature.
Now, for the cyclopropene structure , the number of π electron are equal to 4 , 2 from the double bond and 2 from the negative charge .
Therefore , the compound becomes not aromatic or anti - aromatic .
You might be interested in
Answer : The sketch of two amino acids side by side are shown below.
Explanation :
Amino acid : Amino acid are the acid that contains two functional groups which are carboxylic group, and ammine group,
.
When the two or more that two amino acids join together with the help of peptide bond, they produces polypeptide chain or protein.
The bond present between the two amino acid is called a peptide bond.
The peptide bond is a chemical bond that is formed between the two molecules when the nitrogen of one amino acid react with the carbon of another amino acid by releasing a water molecule.
Hence, the sketch of two amino acids side by side are shown below.
