Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

Write a chemical equation for the formation of methionyl glycine from the constituent amino acids.

Short Answer

Expert verified
\(C_5H_{11}NO_2S\) (Methionine) + \(C_2H_5NO_2\) (Glycine) -> \(C_7H_{14}N_2O_3S\) (Methionyl glycine) + \(H_2O\) (Water)

Step by step solution

01

Identify the constituent amino acids

Methionyl glycine is a dipeptide formed from the condensation of methionine and glycine. Methionine has the chemical formula \(C_5H_{11}NO_2S\) and glycine has the formula \(C_2H_5NO_2\).
02

Write the condensation reaction

The condensation reaction involves the formation of a peptide bond between the carboxyl group of methionine and the amino group of glycine, with the release of a water molecule. The general form of a condensation reaction between two amino acids can be written as: Amino Acid 1 (AA1) + Amino Acid 2 (AA2) -> Dipeptide (AA1-AA2) + Water For our specific case, this is: Methionine + Glycine -> Methionyl glycine + Water
03

Write the full chemical equation

Now, we can plug in the chemical formulas of methionine, glycine, methionyl glycine, and water to write the full chemical equation: \(C_5H_{11}NO_2S\) (Methionine) + \(C_2H_5NO_2\) (Glycine) -> \(C_7H_{14}N_2O_3S\) (Methionyl glycine) + \(H_2O\) (Water)

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

The IUPAC name for a carboxylic acid is based on the name of the hydrocarbon with the same number of carbon atoms. The ending -oic is appended, as in ethanoic acid, which is the IUPAC name for acetic acid. Draw the structure of the following acids: (a) methanoic acid. (b) pentanoic acid, and (c) 2 -chloro-3-methyldecanoic acid

Imagine a single DNA strand containing a section with the following base sequence: \(5^{\prime}\) -GCATTGGC-3'. What is the base sequence of the complementary strand? (The two strands of DNA will come together in an antiparallel fashion: that is, \(5^{\prime}\) - \(\mathrm{TAG}=3^{\prime}\) will bind to \(3^{\prime}\) - \(\mathrm{ATC}-5^{\prime}\).)

Draw the condensed structure of the compounds formed by condensation reactions between (a) benzoic acid and ethanol, (b) ethanoic acid and methylamine, (c) acetic acid and phenol. Name the compound in each case.

(a) Draw the condensed structure of the tripeptide GlyGly-His. (b) How many different tripeptides can be made from the amino acids glycine and histidine? Give the abbreviations for each of these tripeptides, using the three-letter and one-letter codes for the amino acids.

One of the most important molecules in biochemical systems is adenosine triphosphate (ATP), for which the structure is ATP ATP is the principal carrier of biochemical energy. It is considered an energy-rich compound because the hydrolysis of ATP to yield adenosine diphosphate (ADP) and inorganic phosphate is spontaneous under aqueous biochemical conditions. (a) Write a balanced equation for the reaction of ATP with water to yield ADP and inorganic phosphate ion. [Hint: Hydrolysis reactions are just the reverse of condensation reactions(Section 22.8).] (b) What would you expect for the sign of the free-energy change for this reaction? (c) ADP can undergo further hydrolysis. What would you expect for the product of that reaction?

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free