$\text { Myristic acid } \rightarrow \mathrm{CH}_3\left(\mathrm{CH}_2\right)_{12} \mathrm{COOH} \\& \text { Palmitic acid } \rightarrow \mathrm{CH}_3\left(\mathrm{CH}_2\right)_{14} \mathrm{COOH} \\$

Acid palmitic acid has higher melting point, because it has two more methylene groups.

Giving it a greater surface area and therefore more intermolecular van der waals interact than the myristic acid.

stearic arid $\mathrm{CH}_3\left(\mathrm{CH}_2\right)_{16} \mathrm{COOH}$

linoleic acid $\mathrm{C}_{18} \mathrm{H}_{32} \mathrm{O}_2$ (two double bond)

Stearic acid has higher Melting point, because it does not have any Carbon-Carbon double bonds, whereas linoleic acid has two cis double bonds which prevent the molecules from packing closely together.

Oleic Acid and Linoleic acid.

$\mathrm{C}_{18} \mathrm{H}_{34} \mathrm{O}_2$ -one double bond (cis)

Acid palmitic acid has higher melting point, because it has two more methylene groups.

For more such question on methylene group.

brainly.com/question/4279223

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4 0

1 year ago

The actual yield of a product in a reaction was measured as 4.20 g. If the theoretical yield of the product for the reaction is

Dmitry_Shevchenko [17]

Answer:

Explanation:

remember the equation percentage yield = actual/ theoretical yield as

4.20/4.88 x 100

86.065 so 86.1.

hope this make sense:)

3 0

3 years ago

What is the unit for IMA

Tatiana [17]

Answer:

Newton Joules

Explanation:

8 0

3 years ago