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1. Parabens are esters of 4-hydroxybenzoic acid (structure), give example of a paraben & draw other compound used to make it. 2. Suggest a possible use for parabens. 3. What type of hybridisation does the aromatic carbon adopt? 4. How do pi bonds form?

Eg. methyl/ethyl/propyl (etc.) paraben. Drawing of the alcohol used to make paraben. Possible uses: food preservative, cosmetic, or pharmaceutical use. The aromatic carbon atoms are sp²hybridised. p orbitals bond side on/ p orbitals overlap sideways/ suitable diagram.

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1. Parabens are esters of 4-hydroxybenzoic acid (structure), give example of a paraben & draw other compound used to make it. 2. Suggest a possible use for parabens. 3. What type of hybridisation does the aromatic carbon adopt? 4. How do pi bonds form?

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1. Parabens are esters of 4-hydroxybenzoic acid (*structure*), give example of a paraben & draw other compound used to make it. 2. Suggest a possible use for parabens. 3. What type of hybridisation does the aromatic carbon adopt? 4. How do pi bonds form?

Related Chemistry Scottish Highers answers

The formation of ammonia is an equilibrium reaction; N2(g) + 3 H2(g) <--> 2 NH3(g) the enthalpy of this reaction is negative. What can be done to increase the yield of products?

How do you work out the limiting reagent in a reaction?

a.) What is the definition of ionisation energy? b.) Explain trends in ionisation energy within the periodic table

A student obtained 3.7g of methyl cinnamate (162g/mol) from 6.5g of cinnamic acid (148g/mol) and 2.0g of methanol (32g/mol). Determine which reagent is limiting and calculate the percentage yield achieved by the student.

We're here to help

Company Information

Popular Requests

© MyTutorWeb Ltd 2013–2025

CLICK CEOP

1. Parabens are esters of 4-hydroxybenzoic acid (structure), give example of a paraben & draw other compound used to make it. 2. Suggest a possible use for parabens. 3. What type of hybridisation does the aromatic carbon adopt? 4. How do pi bonds form?