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Maximum number of tetrapeptides that can be prepared from the 10 essential amino acids is (a) 10,000 (b) 5000 (c) 2500 (d) 15000

Short Answer

Expert verified
Answer: 10,000 different tetrapeptides can be formed from the 10 essential amino acids.

Step by step solution

01

Understanding the problem

In this problem, we are given 10 different amino acids, from which we need to form tetrapeptides, which are four amino acids linked together. We can use each amino acid more than once, so we need to find all the possible combinations and keep in mind that repetition is allowed.
02

Calculate the number of permutations

We need to use the formula for permutation with repetition, which is given by: n^r where n is the number of items available (10 amino acids) and r is the number of spots to fill (4 spots because it is a tetrapeptide). In our case, n = 10 and r = 4.
03

Perform the calculation

Now we can calculate the possible permutations using the formula, which is: 10^4 = 10000 This means there are 10,000 different tetrapeptides that can be formed from the 10 essential amino acids. So the correct answer is (a) 10,000.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Permutations with Repetition
Understanding the principles of permutations with repetition is key to solving a wide range of combinatorial problems. In problems like forming tetrapeptides that consist of a sequence of amino acids, each position in the sequence can be occupied by any one of the available amino acids, and the same amino acid can occur multiple times in the sequence.

Mathematically, the formula to calculate permutations with repetition is denoted as \( n^r \), where \( n \) represents the number of available different items and \( r \) signifies the number of positions to fill. In the context of our problem, with 10 essential amino acids and 4 positions in a tetrapeptide, we calculate the permutations as \( 10^4 \), which represents all the ways we can arrange these amino acids allowing for duplicates.
Essential Amino Acids
Our bodies need amino acids to synthesize proteins, which are critical to nearly every bodily function. Out of the twenty standard amino acids, there are nine that humans cannot synthesize, known as essential amino acids. These must be obtained through our diet.

These essential amino acids include Histidine, Isoleucine, Leucine, Lysine, Methionine, Phenylalanine, Threonine, Tryptophan, and Valine. Understanding these amino acids is pivotal in biochemistry and for anyone looking to solve problems related to protein synthesis or nutrition.
Protein Structure
Peptides and proteins are fundamental components of cells that carry out important biological functions. A tetrapeptide is a molecule formed by linking together four amino acids with peptide bonds. The sequence and type of amino acids determine the structure and function of the peptide.

Proteins are comprised of one or more polypeptide chains, each folded into a specific three-dimensional structure. This structure is essential for the protein's function. Proteins can have four levels of structure - primary, secondary, tertiary, and quaternary. All these levels of structure influence the final shape and function of the protein in the biological system.
IIT JEE Chemistry Preparation
Students aiming to excel in the IIT JEE, one of India's most challenging engineering entrance exams, must thoroughly understand and practice a broad spectrum of concepts across Physics, Chemistry, and Mathematics. For Chemistry, a strong grasp of organic and inorganic chemistry, including the knowledge of amino acids and protein structure, is essential.

As potential candidates prepare for the exam, practicing combinatorial problems like calculating the number of tetrapeptides can sharpen their problem-solving skills. Furthermore, understanding the underlying principles of chemistry - from molecular interactions to chemical bonding - can provide a significant advantage in achieving success in the IIT JEE.

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Most popular questions from this chapter

Each question in this section has four suggested answers of which ONE OR MORE answers will be correct. Identify the correct statement(s) regarding amino acids and peptides from the following. (a) C-N bond length in peptides is smaller than the usual \(\mathrm{C}-\mathrm{N}\) bond length in amines. (b) Atoms in -CO-NH -group are not in a plane. (c) An important sensitive test for the detection of amino acids is the ninhydrin colour test. (d) The isoelectric point of glutamic acid is about \(3.2\).

Each question in this section has four suggested answers of which ONE OR MORE answers will be correct. Which of the following reactions will give phenyl cyanide as a product? (a) Reaction of benzene diazonium chloride with cuprous cyanide and KCN (b) Heating bromobenzene with alcoholic potassium cyanide (c) Dehydration of benzaldoxime by heating with acetic anhydride (d) Fusing sodium benzene sulphonate with \(\mathrm{NaCN}\)

Sandmeyer reaction, is a type of (a) unimolecular nucleophilic substitution reaction (b) unimolecular electrophilic substitution reaction (c) bimolecular nucleophilic substitution reaction (d) free radical reaction

When \(\mathrm{RNH}_{2}\) is warmed with \(\mathrm{CS}_{2}\) in presence of \(\mathrm{HgCl}_{2}\), RNCS is formed. This is called (a) Hoffmann exhaustive methylation reaction (b) Hoffmann degradation reaction (c) Hoffmann carbylamine reaction (d) Hoffmann mustard oil reaction

How will you convert (a) benzene to \(\mathrm{m}\) -bromo iodobenzene? (b) aniline to \(3,5-\) di iodo nitrobenzene?

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