Answer:
Explanation:
An electrophilic addition reaction occurs when an electrophile attacks a substrate, with the end result being the inclusion of one or many comparatively straightforward molecules along with multiple bonds.
In the given question, the hydrogen bromide provides the electrophile while the bromide is the nucleophile. The mechanism proceeds with the attack of the electrophile on the carbon, followed by deprotonation. This process is continued with a formation of carbocation and the bromide(nucleophile) finally bonds to the carbocation to form a stable product.
The first diagram showcases the possible various starting molecules for the synthesis while the second diagram illustrates their mechanism.
Answer:
The IUPAC name of the compound has already been given which is 2,2-dimethyl-4-ethylheptane.
Explanation:
The IUPAC (International Union of Pure and Applied Chemistry) is an authority in chemistry that provides a guideline and standardized methods in the naming of compounds formed from the periodic table.
In order the give an IUPAC name to a compound, certain steps needs to be followed, these includes:
--> Identify the functional group in the compound as this will form the suffix. For example if the functional group is an alkane the suffix will be -ane.
--> Identify the longest carbon chain (it may not be a straight chain) that contains the functional group. This forms the prefix. Example: if the longest carbon chain is 7 carbon atoms then the prefix will be hept-
--> All the carbons of the longest chain should be numbered
--> Identify branched groups on the chain and name them according to the number of carbon atoms. They usually end with -yl.
--> Finally, combine the elements of the name is a single word.
The structural formula of the IUPAC compound can be found in the attached file for a better understanding. The branched groups are circled.