
But-1-ene reacts with steam as shown to form a mixture of two structural isomers, S and T.

Answer
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Hint: But-1-ene contains a double bond at carbon-1. Whenever but-1-ene reacts with steam it produces two different products (alcohols) in different percentages due to the asymmetrical nature of the but-1-ene.
Complete step by step answer:
- In the question it is given that But-1-ene reacts with steam and produces the products S (major amount0 and product T (minor amount).
- We have to identify the products S and T in the given reaction.
- The chemical reaction of but-1-ene with steam is as follows.
- In the above chemical reaction but-1-ene reacts with steam and forms two types of products.
- The two products are secondary alcohol (major amount) and primary alcohol (minor amount).
- The reason behind the formation of the secondary alcohol in major amounts is the formation of secondary carbocation as an intermediate during the reaction of but-1-ene with steam.
- Secondary carbocation is more stable than the primary carbocation.
- The formed product S (secondary alcohol) further undergoes reaction with potassium dichromate (oxidizing reagent) and forms a ketone as the product.
- The chemical reaction of product S with potassium dichromate is as follows.
- Therefore the product formed when compound ‘S’ is going to react with potassium dichromate is But-2-one (U).
Note: Whenever secondary alcohols react with potassium dichromate ketones are going to form as the product. While primary alcohols react with potassium dichromate and forms aldehyde as the product under reflux conditions.
Complete step by step answer:
- In the question it is given that But-1-ene reacts with steam and produces the products S (major amount0 and product T (minor amount).
- We have to identify the products S and T in the given reaction.
- The chemical reaction of but-1-ene with steam is as follows.

- In the above chemical reaction but-1-ene reacts with steam and forms two types of products.
- The two products are secondary alcohol (major amount) and primary alcohol (minor amount).
- The reason behind the formation of the secondary alcohol in major amounts is the formation of secondary carbocation as an intermediate during the reaction of but-1-ene with steam.
- Secondary carbocation is more stable than the primary carbocation.
- The formed product S (secondary alcohol) further undergoes reaction with potassium dichromate (oxidizing reagent) and forms a ketone as the product.
- The chemical reaction of product S with potassium dichromate is as follows.

- Therefore the product formed when compound ‘S’ is going to react with potassium dichromate is But-2-one (U).
Note: Whenever secondary alcohols react with potassium dichromate ketones are going to form as the product. While primary alcohols react with potassium dichromate and forms aldehyde as the product under reflux conditions.
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