The average molar mass of one base pair of nucleotides in DNA is approximately 600 g/mol. The spacing between successive base pairs is about $0.34 \mathrm{nm},$ and a complete turn in the helical structure of DNA occurs about every 3.4 \(\mathrm{nm}\) . If a DNA molecule has a molar mass of $4.5 \times 10^{9} \mathrm{g} / \mathrm{mol}$ , approximately how many complete turns exist in the DNA \(\alpha\) -helix structure?

Short Answer

Expert verified
There are approximately 750,000 complete turns in the DNA 𝛼-helix structure.

Step by step solution

01

Calculate the number of base pairs

To calculate the number of base pairs in the DNA molecule, we divide the molar mass of the DNA molecule by the average molar mass of one base pair. We can write this as: Number of base pairs = (Molar mass of DNA molecule) / (Average molar mass of one base pair) Number of base pairs = (4.5 * 10^9 g/mol) / (600 g/mol) Number of base pairs ≈ 7.5 * 10^6
02

Calculate the length of the DNA molecule

Now, we will find the length of the DNA molecule. For this, we will multiply the number of base pairs by the spacing between successive base pairs: Length of DNA molecule = (Number of base pairs) * (Spacing between successive base pairs) Length of DNA molecule ≈ (7.5 * 10^6) * 0.34 nm Length of DNA molecule ≈ 2.55 * 10^6 nm
03

Calculate the number of complete turns

Finally, we need to determine how many complete turns exist in the DNA 𝛼-helix structure. To do this, we will divide the length of the DNA molecule by the length per turn: Number of complete turns = (Length of DNA molecule) / (Length per turn) Number of complete turns ≈ (2.55 * 10^6 nm) / (3.4 nm) Number of complete turns ≈ 750,000 So, there are approximately 750,000 complete turns in the DNA 𝛼-helix structure.

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

Why is glycine not optically active?

For each of the following, fill in the blank with the correct response. All of these fill-in-the-blank problems pertain to material covered in the sections on alkanes, alkenes and alkynes, aromatic hydrocarbons, and hydrocarbon derivatives. a. The first “organic” compound to be synthesized in the laboratory, rather than being isolated from nature, was , which was prepared from . b. An organic compound whose carbon–carbon bonds are all single bonds is said to be . c. The general orientation of the four pairs of electrons around the carbon atoms in alkanes is . d. Alkanes in which the carbon atoms form a single unbranched chain are said to be alkanes. e. Structural isomerism occurs when two molecules have the same number of each type of atom but exhibit different arrangements of the between those atoms. f. The systematic names of all saturated hydrocarbons have the ending added to a root name that indicates the number of carbon atoms in the molecule. g. For a branched hydrocarbon, the root name for the hydrocarbon comes from the number of carbon atoms in the continuous chain in the molecule. h. The positions of substituents along the hydrocarbon framework of a molecule are indicated by the of the carbon atom to which the substituents are attached. i. The major use of alkanes has been in reactions, as a source of heat and light. j. With very reactive agents, such as the halogen elements, alkanes undergo reactions, whereby a new atom replaces one or more hydrogen atoms of the alkane. k. Alkenes and alkynes are characterized by their ability to undergo rapid, complete reactions, by which other atoms attach themselves to the carbon atoms of the double or triple bond. l. Unsaturated fats may be converted to saturated fats by the process of . m. Benzene is the parent member of the group of hydrocarbons called hydrocarbons. n. An atom or group of atoms that imparts new and characteristic properties to an organic molecule is called a group. o. A alcohol is one in which there is only one hydrocarbon group attached to the carbon atom holding the hydroxyl group. p. The simplest alcohol, methanol, is prepared industrially by the hydrogenation of . q. Ethanol is commonly prepared by the of certain sugars by yeast. r. Both aldehydes and ketones contain the group, but they differ in where this group occurs along the hydrocarbon chain. s. Aldehydes and ketones can be prepared by of the corresponding alcohol. t. Organic acids, which contain the group, are typically weak acids. u. The typically sweet-smelling compounds called result from the condensation reaction of an organic acid with an .

Identify each of the following compounds as a carboxylic acid, ester, ketone, aldehyde, or amine. a. Anthraquinone, an important starting material in the manufacture of dyes:

Glucose can occur in three forms: two cyclic forms and one open-chain structure. In aqueous solution, only a tiny fraction of the glucose is in the open-chain form. Yet tests for the presence of glucose depend on reaction with the aldehyde group, which is found only in the open-chain form. Explain why these tests work.

Poly(lauryl methacrylate) is used as an additive in motor oils to counter the loss of viscosity at high temperature. The structure is The long hydrocarbon chain of poly(lauryl methacrylate) makes the polymer soluble in oil (a mixture of hydrocarbons with mostly 12 or more carbon atoms). At low temperatures the polymer is coiled into balls. At higher temperatures the balls uncoil and the polymer exists as long chains. Explain how this helps control the viscosity of oil.

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