Subject

Biology

Class

NEET Class 12

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 Multiple Choice QuestionsMultiple Choice Questions

71.

Limit of BOD prescribed by Central Pollution Control Board for the discharge of industrial and municipal waste water into natural surface water, is:

  • < 3.0 ppm

  • < 10 ppm

  • < 100 ppm

  • < 100 ppm

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72.

Withdrawal of which of the following hormones is the immediate cause of menstruation?

  • Eastrogens

  • FSH

  • FSH-RH

  • FSH-RH

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73.

The arrangement of the nuclei in a normal embryo sac in the dicot plants is

  • 2+4+2

  • 3+2+3

  • 2+3+3

  • 2+3+3

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74.

An enzyme that can stimulate germination of barley seeds is

  • α-amylase

  • lipase

  • protease

  • protease

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75.

In a cereal grain the single cotyledon of embryo is represented by

  • coleorhiza

  • scutellum

  • prophyll

  • prophyll

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76.

Triticale, the first man-made cereal crop, has been obtained by crossing wheat with

  • rye

  • pearl millet

  • sugarcane

  • sugarcane

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77.

In order to obtain virus-free plants through tissue culture the best method is

  • protoplast culture

  • embryo rescue

  • anther culture

  • anther culture

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78.

HIV that causes AIDS, first starts destroying

  • B-lymphocytes

  • leucocytes

  • thrombocytes

  • thrombocytes

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79.

Sickle cell anaemia has not been eliminated from the African population because

  • it is controlled by recessive genes

  • it is not a fatal disease

  • it provides immunity against malaria

  • it provides immunity against malaria

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80.

Both sickle cell anaemia and Huntington's chorea are

  • bacteria-related diseases

  • congenital disorders

  • pollutant-induced disorders

  • pollutant-induced disorders


B.

congenital disorders

Both sickle cell anaemia and Huntington's chorea are congenital genetic disorders. Sickle cell anaemia was first opened by James Herrick (1904). In this disease the patient's haemoglobin level reduced to half of the normal and the RBCs become sickle shaped. A single mutation in a gene can cause sickle cell anaemia.
Huntington's chorea is caused by autosomal mutation which is dominant. The gene is present on chromosome number 4.

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