ATI TEAS 7
ATI TEAS Science Questions
1. If a patient had a heart attack and tissue in the left ventricle lost blood flow, what would you most expect to happen?
- A. Blood would not flow from the lungs.
- B. Blood would back up in the legs.
- C. Blood would not be pumped to the body.
- D. Blood would not be oxygenated.
Correct answer: C
Rationale: The correct answer is C: 'Blood would not be pumped to the body.' When tissue in the left ventricle loses blood flow due to a heart attack, the ability of the left ventricle to pump oxygenated blood to the body is compromised. This can lead to serious consequences for the patient's overall health and organ function. Choices A, B, and D are incorrect because a heart attack affecting the left ventricle does not directly impact blood flow from the lungs, cause blood to back up in the legs, or prevent blood from being oxygenated. The primary concern is the compromised ability of the left ventricle to pump blood to the rest of the body, affecting overall circulation and organ perfusion.
2. What is the term for the number of moles of solute per liter of solution?
- A. Molarity
- B. Molality
- C. Normality
- D. Concentration
Correct answer: A
Rationale: Molarity is the correct term for the number of moles of solute per liter of solution. It is expressed as moles of solute divided by liters of solution. Molality (B) is similar but is moles of solute per kilogram of solvent. Normality (C) is the number of equivalents of solute per liter of solution, and Concentration (D) is a general term for the amount of solute present in a given quantity of solution. Therefore, the correct answer is A, molarity, as it specifically refers to moles of solute per liter of solution.
3. What type of macromolecule is hemoglobin?
- A. Carbohydrate
- B. Lipid
- C. Protein
- D. Nucleic acid
Correct answer: C
Rationale: The correct answer is C: Protein. Hemoglobin is a protein responsible for carrying oxygen in the blood. Proteins are macromolecules made up of amino acids and play a vital role in various biological functions, including the transportation of molecules like oxygen. Choices A, B, and D are incorrect because carbohydrates, lipids, and nucleic acids are different types of macromolecules that have distinct structures and functions. Carbohydrates are mainly involved in energy storage and structural support, lipids are essential for energy storage and cell membrane structure, and nucleic acids are responsible for storing and transmitting genetic information.
4. What is the ultimate end product of glucose breakdown in glycolysis?
- A. ATP
- B. NADPH
- C. Pyruvic acid
- D. Oxygen
Correct answer: C
Rationale: The ultimate end product of glucose breakdown in glycolysis is pyruvic acid. During glycolysis, glucose is broken down into pyruvic acid through a series of enzymatic reactions. ATP is produced as an energy carrier during glycolysis, but it is not the final end product. NADPH is not a direct product of glycolysis; it is mainly produced in the pentose phosphate pathway. Oxygen is not a product of glycolysis but is used as an electron acceptor in the electron transport chain of cellular respiration.
5. What type of genetic testing can reveal an individual's susceptibility to certain diseases?
- A. Karyotyping
- B. Pharmacogenomics
- C. Paternity testing
- D. Microarray analysis
Correct answer: D
Rationale: A) Karyotyping is a genetic test that examines an individual's chromosomes to detect abnormalities such as extra or missing chromosomes. It is not typically used to reveal an individual's susceptibility to certain diseases. B) Pharmacogenomics is the study of how genes affect a person's response to drugs. It focuses on how genetic variations can influence drug response, rather than susceptibility to diseases. C) Paternity testing is a genetic test used to determine the biological relationship between a child and an alleged father. It is not used to reveal an individual's susceptibility to diseases. D) Microarray analysis is a type of genetic testing that can reveal an individual's susceptibility to certain diseases by analyzing variations in their DNA. It can identify genetic markers associated with increased risk for specific conditions, allowing for personalized risk assessment and preventive measures.
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