Question

1. 1-propanol can form __________ with _______, but butane cannot.2. 1-propanol is more soluble than ethyl methyl ether because it can form more _______ with _______.3. Ethanol is more soluble in water than 1-hexanol because it has ______.

Answer 1

1-propanol can form hydrogen bonds with water, unlike butane. This ability for hydrogen bonding also makes 1-propanol more soluble in water than ethyl methyl ether. Ethanol's solubility benefits from having fewer carbon atoms, which enhances its hydrogen bonding capability with water compared to 1-hexanol.

Step-by-step explanation:

1. 1-propanol can form hydrogen bonds with water molecules, but butane cannot.

2. 1-propanol is more soluble than ethyl methyl ether because it can form more hydrogen bonds with water molecules.

3. Ethanol is more soluble in water than 1-hexanol because it has fewer carbon atoms, allowing for more effective hydrogen bonding with water due to a lesser effect from the nonpolar hydrocarbon chain.

Answer 2

Answe:

1. 1-propanol can form Hydrogen Bonds with other alcohol molecules but butane cannot.

2. 1-propanol is more soluble than ethyl methyl ether because it can form more hydrogen bonds with water.

3. Ethanol is more soluble in water than 1-hexanol because it has ethanol has shorter carbon chain whereas 1-hexanol has longer carbon chains.

Step-by-step explanation:

Propanol can react with other alcohol molecules through hydrogen bonding to form ethers because alcohols do not dehydrate to form alkenes. They do this through that Williamson Ether Synthesis. In other words, alcohols can serve as an acid and a base in reactions. Butane do not follow this process.

Propanol can form hydrogen bonds with water making it more soluble than ethyl methyl ether. Propanol can donate and accept electrons which makes them interact with water better than ethyl methyl ether which can only receive proton from water.

Ethanol is mode soluble than hexanol beacuse it's non polar chain is shorter unlike in hexanol with a longer chain. Both alcohols has hydoxyl group which makes them soluble in water but their solubility is greatly affected by the remaining non polar side of the alcohol. Long non polar chain reduces solubility and vice versa.