Nokea
Which element has the lowest electronegativity value?
- A. Oxygen
- B. Fluorine
- C. Helium
- D. Chlorine
Correct Answer: C
Rationale: The correct answer is Helium (C). Electronegativity is the tendency of an atom to attract electrons towards itself in a bond. Helium, as a noble gas, has a very low electronegativity because its outer electron shell is already full and stable, resulting in minimal attraction for additional electrons. Oxygen (A), Fluorine (B), and Chlorine (D) are all non-noble gas elements that have higher electronegativity values compared to Helium due to their electron configurations and tendencies to attract electrons.
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Deuterium, a stable isotope of hydrogen, has a nucleus containing:
- A. A single proton
- B. A proton and a neutron
- C. Two protons and an electron
- D. Two neutrons
Correct Answer: B
Rationale: Deuterium, as an isotope of hydrogen, has an atomic number of 1 and a mass number of 2. The nucleus of deuterium contains one proton (as in all hydrogen atoms) and one neutron, totaling 2 nucleons in the nucleus. Therefore, the correct answer is that deuterium's nucleus contains a proton and a neutron. Choices A, C, and D are incorrect. Deuterium is not just a single proton (A), doesn't have two protons and an electron (C), and doesn't contain two neutrons (D). The correct composition of deuterium's nucleus is one proton and one neutron.
What condition is characterized by progressive muscle weakness and wasting?
- A. Muscular dystrophy
- B. Myositis
- C. Fibromyalgia
- D. Carpal tunnel syndrome
Correct Answer: A
Rationale: Muscular dystrophy is a genetic disorder characterized by progressive muscle weakness and wasting due to mutations in genes responsible for muscle cells' structure and function. Myositis is an inflammatory muscle disease, fibromyalgia is a chronic pain condition, and carpal tunnel syndrome affects the hand and arm nerves, but none present with the progressive muscle weakness and wasting seen in muscular dystrophy.
When referring to blood vessel walls, the term 'atherosclerosis' describes:
- A. The abnormal buildup of plaque within the arterial walls.
- B. The inflammation of the inner lining of blood vessels.
- C. The dilation and weakening of a blood vessel wall (aneurysm).
- D. The normal process of blood vessel wall thickening with age.
Correct Answer: A
Rationale: The correct answer is A: 'The abnormal buildup of plaque within the arterial walls.' Atherosclerosis is the process where plaque, consisting of fat, cholesterol, calcium, and other substances, accumulates within the arteries. This buildup can lead to the hardening and narrowing of arteries, reducing blood flow and potentially causing severe health issues like heart attacks and strokes. Choice B is incorrect because inflammation of the inner lining of blood vessels is known as vasculitis, not atherosclerosis. Choice C is incorrect as it describes an aneurysm, which is a dilation and weakening of a blood vessel wall, not atherosclerosis. Choice D is incorrect as it describes arteriosclerosis, a process of blood vessel wall thickening with age, which is different from atherosclerosis.
What is the term for a genetic disorder caused by a mutation in a mitochondrial gene?
- A. Autosomal dominant disorder
- B. Autosomal recessive disorder
- C. Sex-linked disorder
- D. Mitochondrial disorder
Correct Answer: D
Rationale: A) Autosomal dominant disorder: This type of genetic disorder is caused by a mutation in one copy of an autosomal gene. It is not related to mitochondrial gene mutations. B) Autosomal recessive disorder: This type of genetic disorder is caused by mutations in both copies of an autosomal gene. It is not related to mitochondrial gene mutations. C) Sex-linked disorder: This type of genetic disorder is caused by mutations in genes located on the sex chromosomes (X or Y). It is not related to mitochondrial gene mutations. D) Mitochondrial disorder: Mitochondrial disorders are genetic disorders caused by mutations in genes located in the mitochondria, the energy-producing structures within cells. These disorders are inherited maternally and can affect various organs and systems in the body due to the role of mitochondria in energy production.
During embryonic development, most vertebrates exhibit structures called pharyngeal pouches. These pouches eventually develop into different structures in various vertebrate groups, such as the human jaw and inner ear. Pharyngeal pouches are an example of:
- A. Analogous structures with different evolutionary origins but similar functions
- B. Homologous structures with a common evolutionary origin but diverse functions
- C. Vestigial structures that no longer serve a vital function in some organisms
- D. Atavisms, the reappearance of a trait absent in recent generations
Correct Answer: B
Rationale: Pharyngeal pouches in vertebrates are an example of homologous structures because they share a common evolutionary origin. Despite developing into different structures in various vertebrate groups, such as the jaw and inner ear in humans, these structures originated from the same ancestral feature. This concept of homology highlights the evolutionary relationship between different species and how structures can be modified over time to serve different functions while retaining a common origin. Choice A is incorrect because analogous structures have similar functions but different evolutionary origins, which does not apply to pharyngeal pouches. Choice C is incorrect as vestigial structures are remnants of features that were functional in ancestors but have reduced or lost their original function, which is not the case for pharyngeal pouches. Choice D is incorrect because atavisms refer to the reappearance of traits absent in recent generations, which is not the characteristic of pharyngeal pouches.