Class: 12 (2025-26)
CLASS TEST
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TIME: 2 HOURS |
M.M.: 50 |
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General Instructions:
• This question paper
contains 22 questions.
• All questions are
compulsory.
• Q.1 to 5 (Multiple Choice
Questions (MCQs)): 5 questions. Each question carries 1 mark.
• Q.6 to 7 (Assertion Reason
Questions): 2 questions. Each question carries 1 mark.
• Q.8 to 11 (Very Short
Answer Questions): 4 questions. Each question carries 1 mark.
• Q.12 to 16 (Short Answer
Questions): 5 questions. Each question carries 2 marks.
• Q.17 to 21 (Long Answer
Questions): 5 questions. Each question carries 5 marks.
• Q.22 to 22 (Competency
Based Questions): 1 questions. Each question carries 4 marks.
Topics Covered:
• Principles of Inheritance
and Variation
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Q.NO. |
QUESTIONS |
MARKS |
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MULTIPLE CHOICE QUESTIONS (MCQS) Questions 1 to 5 (5 questions × 1 mark each) |
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1 |
In Mendelian inheritance, which law
states that alleles of different genes assort independently of one another
during gamete formation? A. Law of Segregation B. Law of Dominance C. Law of Independent Assortment D. Law of Recombination |
1 |
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2 |
A plant with genotype TtYy is crossed
with a plant with genotype Ttyy. What is the probability of obtaining an
offspring with genotype TtYy? A. 1/4 B. 1/2 C. 1/8 D. 1/16 |
1 |
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3 |
Which of the following genetic
disorders is caused by a mutation in a single gene? A. Down Syndrome B. Turner Syndrome C. Sickle Cell Anemia D. Klinefelter Syndrome |
1 |
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4 |
In a dihybrid cross involving two
heterozygous parents (AaBb x AaBb), what is the expected phenotypic ratio in
the F1 generation? A. 9:3:3:1 B. 1:1:1:1 C. 3:1 D. 1:2:1 |
1 |
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5 |
A woman with blood group AB marries a
man with blood group O. What is the probability that their child will have
blood group A? A. 0% B. 25% C. 50% D. 75% |
1 |
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ASSERTION REASON QUESTIONS Questions 6 to 7 (2 questions × 1 mark each) Instructions: The
following questions consist of two statements – Assertion (A) and Reason (R). Answer
these questions by selecting the appropriate option given below: A.
Both A and R are true, and R is the correct explanation of A. B.
Both A and R are true, and R is not the correct explanation of A. C.
A is true but R is false. D.
A is false but R is true. |
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6 |
Assertion (A): In Mendelian
inheritance, the F2 generation shows a phenotypic ratio of 3:1 in a
monohybrid cross. Reason (R): The F1
generation produces gametes with two different alleles in equal proportions. |
1 |
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7 |
Assertion (A): Codominance results in
offspring with a phenotype that is distinct from both parents. Reason (R): In codominance, both alleles in
a heterozygote are fully expressed. |
1 |
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VERY SHORT ANSWER QUESTIONS Questions 8 to 11 (4 questions × 1 mark each) |
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8 |
Define incomplete dominance with an
example. |
1 |
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9 |
What is the phenotypic ratio observed
in the F2 generation of a monohybrid cross? A. 3:1 B. 1:2:1 C. 9:3:3:1 D. 1:1 |
1 |
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10 |
Explain why Mendelian inheritance
patterns may not always be observed in all organisms. |
1 |
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11 |
Assertion (A): The law of independent
assortment is always applicable. Reason
(R): Genes located on the same chromosome assort independently. |
1 |
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SHORT ANSWER QUESTIONS Questions 12 to 16 (5 questions × 2 marks each) |
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12 |
Explain Mendel's law of segregation
using the concept of alleles. |
2 |
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13 |
How does incomplete dominance differ
from codominance? Provide an example of each. |
2 |
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14 |
Describe the significance of test
crosses in genetic studies. |
2 |
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15 |
Compare the mechanisms of sex
determination in cockroaches and Drosophila, highlighting one key difference
in their chromosomal systems. |
2 |
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16 |
Explain how polygenic inheritance
contributes to continuous variation in traits. |
2 |
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LONG ANSWER QUESTIONS Questions 17 to 21 (5 questions × 5 marks each) |
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17 |
Explain the significance of Mendel's
dihybrid cross experiment in establishing the Law of Independent Assortment.
Discuss how this principle is violated during gene linkage. |
5 |
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18 |
A plant with genotype AaBb (where
A=Tall, a=dwarf; B=Red flowers, b=white) was test crossed. The progeny showed
42% parental types and 8% recombinants each for Ab & aB. (a) Calculate
the map distance between these genes (b) Explain why the recombination
frequency isn't 50% |
5 |
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19 |
Compare and contrast incomplete
dominance and codominance using specific examples. How do these phenomena
challenge Mendel's principle of dominance? |
5 |
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20 |
Explain the phenomenon of pleiotropy
with a suitable example. Discuss how pleiotropy influences the inheritance
patterns of genetic disorders and provide insights into its implications for
genetic counseling. |
5 |
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21 |
Describe the chromosomal theory of
inheritance with experimental evidence. How did Morgan's work with Drosophila
provide crucial support for this theory? |
5 |
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COMPETENCY BASED QUESTIONS Questions 22 to 22 (1 questions × 4 marks each) |
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22 |
Down syndrome, Klinefelter syndrome,
and Turner syndrome are genetic disorders resulting from chromosomal
abnormalities. Down syndrome is characterized by trisomy of chromosome 21,
Klinefelter syndrome by the presence of an extra X chromosome in males (47,XXY),
and Turner syndrome by the absence of one X chromosome in females (45,X).
Analyze the genetic constitution and phenotypic characteristics of
individuals with these syndromes. A. Explain how non-disjunction during meiosis leads to the
chromosomal abnormalities observed in Down syndrome, Klinefelter syndrome,
and Turner syndrome. B. Compare and contrast the phenotypic characteristics of
individuals with Down syndrome, Klinefelter syndrome, and Turner syndrome. C. Evaluate the impact of these syndromes on fertility and
reproductive health. D. Discuss the genetic counseling considerations for families
with a history of these syndromes. E. Propose a strategy for early diagnosis and management of these
genetic disorders. |
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