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800 most-asked Class 11 & 12 (+1 / +2) questions across Physics, Chemistry, Maths and Biology — each with a model answer and the exact marking-scheme points examiners reward. Revise smart, walk in calm.
BiologyClass 123 marksmedium
Principles of Inheritance and Variation
What are sex-linked disorders? Explain haemophilia and colour blindness.
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Sex-linked disorders are genetic disorders caused by genes located on the sex chromosomes (usually the X chromosome), so their inheritance is linked to the sex of the individual. Haemophilia is an X-linked recessive disorder in which the blood does not clot properly (a clotting factor is missing), so there is prolonged bleeding even from minor injuries. Colour blindness (red-green) is also an X-linked recessive disorder in which a person cannot distinguish between red and green colours. Because these genes are on the X chromosome, such disorders are more common in males (who have only one X chromosome).
Marking-scheme points
- ✓Caused by recessive genes on the X chromosome
- ✓Haemophilia: blood fails to clot (prolonged bleeding)
- ✓Colour blindness: cannot distinguish red and green; both more common in males
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Molecular Basis of Inheritance
What is semiconservative DNA replication? Briefly describe it.
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Semiconservative replication is the method of DNA replication in which each of the two strands of the parent DNA acts as a template, and the newly formed DNA molecule contains one old (parental) strand and one newly synthesised strand. During replication, the enzyme helicase unwinds and separates the two strands; then the enzyme DNA polymerase adds new nucleotides to each template strand following complementary base pairing, forming two identical daughter DNA molecules. This mode was experimentally proved by Meselson and Stahl.
Marking-scheme points
- ✓Each parent strand acts as a template
- ✓Each daughter DNA has one old and one new strand (semiconservative)
- ✓Helicase unwinds; DNA polymerase adds nucleotides (proved by Meselson and Stahl)
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Molecular Basis of Inheritance
What is transcription? Name the enzyme involved.
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Transcription is the process of copying the genetic information from one strand of DNA into a molecule of messenger RNA (mRNA). Only one strand of the DNA (the template strand) is copied. The enzyme RNA polymerase binds to the promoter region and moves along the template, adding ribonucleotides according to complementary base pairing (A of DNA pairs with U of RNA, and so on), forming the RNA. The three steps are initiation, elongation and termination. In eukaryotes the RNA is then processed (splicing) before it leaves the nucleus.
Marking-scheme points
- ✓Copying genetic information from DNA template into mRNA
- ✓Enzyme: RNA polymerase (binds to the promoter)
- ✓In RNA, adenine pairs with uracil (U); steps: initiation, elongation, termination
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Molecular Basis of Inheritance
What is translation? Briefly describe the process of protein synthesis.
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Evolution
State the Hardy-Weinberg principle and write its equation.
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Human Health and Disease
What is immunity? Distinguish between innate and acquired immunity.
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Microbes in Human Welfare
How do microbes help in sewage treatment? Describe the primary and secondary treatment.
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Biotechnology: Principles and Processes
State the main steps involved in making a recombinant DNA and expressing it.
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Organisms and Populations
Name and briefly explain the different types of population interactions.
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Ecosystem
Explain the flow of energy in an ecosystem and the ten per cent law.
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Biodiversity and Conservation
Distinguish between in-situ and ex-situ conservation of biodiversity with examples.
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