Concept explainers
(a)
Interpretation:
The role of hydrophobic interactions in stabilizing the double-stranded DNA has to be discussed.
Concept Introduction:
The groups which are not present in contact with the aqueous medium (or) which repels the water molecules are said to be hydrophobic in nature.
The DNA molecule is made up of nucleotides which consist of Nitrogenous bases, Sugar molecules and Phosphate ions. The Nitrogenous bases are two types: Purines and Pyrimidines. The Purine bases are Adenine and Guanine. The Pyrimidine bases are Cytosine and Thymine. In the formation of the DNA molecule the bases are paired with each other (Purine base with Pyrimidine base). The pairing occurs as A-T and G-C, the Adenine base containing
(b)
Interpretation:
The role of hydrophobic interactions in stabilizing the Lipid bilayers has to be discussed.
Concept Introduction:
The groups which are not present in contact with the aqueous medium (or) which repels the water molecules are said to be hydrophobic in nature.
The lipid bilayer is a thin polar membrane made up of two layers of lipid molecules. The lipid bilayer is the major constituent in the cell membrane (or) plasma membrane of the cells, which is selectively permeable.
(c)
Interpretation:
The role of hydrophobic interactions in stabilizing the Soap micelles has to be discussed.
Concept Introduction:
The groups which are not present in contact with the aqueous medium (or) which repels the water molecules are said to be hydrophobic in nature.
The soap micelle is defined as when the soapy water is mixed with grease or dirt, the soap molecules forms tiny clusters which are called as micelles.

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Chapter 28 Solutions
EP ORGANIC CHEMISTRY-OWL V2 ACCESS
- Please help me solve this reaction.arrow_forwardIndicate the products obtained by mixing 2,2-dimethylpropanal with acetaldehyde and sodium ethoxide in ethanol.arrow_forwardSynthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Synthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- If possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forward
- We mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forwardIndicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forward
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