Answer:
Explanation:
If we look at the structure of 1-Bromopropane; we will see that it is a derivative of alkane family by the the substitution of an alkyl group. The position of the Bromine in the propane is 1, making 1-Bromopropane a primary alkyl-halide.
Primary alkyl - halide undergo SN2 mechanism. This nucleophilic reaction needs to be a strong alkyl halide , such as 1-Bromopropane used otherwise it will result to a reactive mechanism if a weak electrophile is used.
However, the critical and the main objective here is to Draw the major substitution product if the reaction proceeds in good yield. If no reaction is expected or yields will be poor, draw the starting material in the box. If a charged product is formed, be sure to draw the counterion.
The attached diagrams portraying this notions is shown in the attached file below.
When formaldehyde and acetone then react with each other( aldol condensation) then it will be formed <u> methyl vinyl ketone.</u>
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In organic chemistry, an aldol condensation would be a condensation reaction in which an enol and enolate ion combines with a carbonyl chemical to produce a -hydroxy aldehyde or -hydroxy ketone, that is then dehydrated to produce a conjugated enone.
In aldol condensation, when formaldehyde and acetone then react with each other then it will be formed <u> </u><u>methyl vinyl ketone.</u>
It can be written as
→ 
When it will be heated then it gives methyl vinyl ketones.
→ 
So, the pair of reactants will be formaldehyde and acetone
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Answer:
An amide may be produced by reacting an acid chloride with ammonia.
Answer:
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a pure substance consists only of one element or one compound. a mixture consists of two or more different substances, not chemically joined together.
Explanation:
