Exam Prep13 min read

NEET Cell Structure: 30 Practice Questions with Answers

By the QUFF Team

Cell Structure is foundational in the literal sense - its content resurfaces in Genetics through chromosomes and meiosis, in Plant Physiology through chloroplasts and mitochondria, and in Human Physiology through membranes and transport. It also rewards precision more than most units, because its questions ask which organelle, which stage or which structure rather than for an explanation.

A pie chart, a rising bar graph, a lightbulb and gears on a light background, representing structured biological analysis

Why precision matters more here

Most NEET Biology questions reward understanding a process. Cell Structure questions frequently reward knowing a specific fact - that ribosomes in mitochondria are 70S rather than 80S, that crossing over happens in prophase I rather than prophase II, that lysosomes are formed by the Golgi apparatus.

That makes it a unit where careful reading of NCERT, including the labelled diagrams, pays more directly than in units where the reasoning can be reconstructed. It is also why active recall works particularly well here - there is a defined set of facts to become retrievable.

How NEET actually asks Cell Structure

NTA publishes no chapter-wise weightage for NEET, so figures circulating online are coaching estimates from past papers; check the official NTA information bulletin for the current paper structure.

Recurring types include: identify an organelle from its function or structure, distinguish prokaryotic from eukaryotic features, identify a stage of mitosis or meiosis from a description or diagram, and track chromosome and DNA content through the cell cycle. Matching and assertion-reason formats are common.

Key concepts, compressed

  • The cell theory states that all organisms are made of cells and that all cells arise from pre-existing cells.
  • Prokaryotes lack a true nucleus and membrane-bound organelles; eukaryotes have both.
  • The plasma membrane is a fluid mosaic of lipids and proteins, selectively permeable and capable of lateral movement.
  • Each organelle has a defined function, and questions test the match rather than the mechanism.
  • The nucleus contains chromatin, which condenses into chromosomes during division.
  • The cell cycle alternates interphase, where growth and DNA replication occur, with the M phase of division.

Facts worth fixing before the questions

Confirm all structural details against the current NCERT diagrams, which are examined directly.
ItemDetailNote
Prokaryotic ribosomes70Salso in mitochondria and chloroplasts
Eukaryotic cytoplasmic ribosomes80S
Bacterial cell wallpeptidoglycanplant wall is cellulose
Plant-only structurescell wall, chloroplast, large vacuole
Animal-prominent structurescentrioles, lysosomes
Rough ERprotein synthesisbears ribosomes
Smooth ERlipid synthesisno ribosomes
Golgi apparatusmodifies, packages, forms lysosomes
Lysosomehydrolytic enzymesthe suicidal bag
Mitochondrioncristae, matrix, own DNAsemi-autonomous
Chloroplastthylakoid and stromasemi-autonomous
Crossing overprophase I of meiosisnot prophase II
Reduction divisionmeiosis Inot meiosis II
Cell cycle orderG1, S, G2, MS phase replicates DNA

The five mistakes that cost the most marks

  • Placing crossing over in the wrong stage. It occurs in prophase I of meiosis, not in prophase II and not in mitosis.
  • Thinking meiosis II halves the chromosome number. Meiosis I is the reduction division; meiosis II separates sister chromatids.
  • Confusing chromatid number with chromosome number. A chromosome with two chromatids is still one chromosome.
  • Assuming prokaryotes have no internal structures at all. They lack membrane-bound organelles but have ribosomes, a nucleoid and often plasmids.
  • Assigning ribosome sizes wrongly. Mitochondria and chloroplasts have 70S ribosomes like prokaryotes, not the 80S of the eukaryotic cytoplasm.

Practice set 1: cell theory and cell types

1. What does the cell theory state?

That all living organisms are composed of cells and their products, and that all cells arise from pre-existing cells. Schleiden and Schwann proposed the first two parts, and Virchow added the third, which ruled out spontaneous generation. Viruses are the recognised exception, since they are acellular.

2. What are the main differences between prokaryotic and eukaryotic cells?

Prokaryotes lack a nuclear membrane and membrane-bound organelles, have a single circular chromosome in a nucleoid, and carry 70S ribosomes. Eukaryotes have a true nucleus, membrane-bound organelles, multiple linear chromosomes and 80S cytoplasmic ribosomes. Prokaryotes are also generally much smaller.

3. What is the difference between 70S and 80S ribosomes?

70S ribosomes are found in prokaryotes and also inside mitochondria and chloroplasts; 80S ribosomes are found in the eukaryotic cytoplasm. The S refers to the sedimentation coefficient, which is why the subunit values do not add arithmetically - 50S and 30S combine to give 70S.

4. How do bacterial and plant cell walls differ in composition?

Bacterial cell walls are made of peptidoglycan, a polymer of sugars and amino acids. Plant cell walls are made of cellulose. Fungal walls contain chitin. This difference matters medically, because antibiotics such as penicillin target peptidoglycan synthesis and therefore harm bacteria without affecting human cells.

5. What structures are found in plant cells but not animal cells?

A cellulose cell wall, chloroplasts and a large central vacuole. Animal cells characteristically have centrioles and prominent lysosomes. Note the framing carefully - some structures are present in both but far more prominent in one, and NEET questions often turn on that distinction.

6. What are the nucleoid, plasmids and mesosomes?

The nucleoid is the region containing the bacterial chromosome, with no surrounding membrane. Plasmids are small circular DNA molecules carrying accessory genes such as antibiotic resistance. Mesosomes are infoldings of the plasma membrane that increase surface area for respiration and other functions. All three demonstrate that prokaryotes are organised without being compartmentalised.

Practice set 2: membrane and organelles

7. Describe the fluid mosaic model of the plasma membrane.

A lipid bilayer in which proteins are embedded - some spanning the membrane as integral proteins, others attached at the surface as peripheral proteins. Fluid refers to the lateral movement of both lipids and proteins within the layer; mosaic refers to the scattered protein distribution. The model explains selective permeability and membrane fusion.

8. Describe the structure and function of mitochondria.

A double membrane, with the inner membrane folded into cristae that increase surface area, enclosing the matrix. The Krebs cycle occurs in the matrix and the electron transport system on the inner membrane. It is the site of aerobic respiration and ATP production, and it is semi-autonomous, having its own circular DNA and 70S ribosomes.

9. Describe the structure of a chloroplast.

A double membrane enclosing the stroma, within which thylakoid membranes are stacked into grana. Light reactions occur on the thylakoid membranes, and the Calvin cycle in the stroma. Like mitochondria it is semi-autonomous, with circular DNA and 70S ribosomes - a point that connects directly to endosymbiotic theory.

10. What is the difference between rough and smooth endoplasmic reticulum?

Rough ER bears ribosomes on its surface and is the site of protein synthesis and processing. Smooth ER lacks ribosomes and is involved in lipid and steroid synthesis and detoxification. Cells specialising in secretion have abundant rough ER, while those in the liver and gonads have abundant smooth ER.

11. What does the Golgi apparatus do?

It modifies, sorts and packages proteins and lipids received from the endoplasmic reticulum, and forms lysosomes and secretory vesicles. It has a distinct polarity - a cis face receiving material and a trans face dispatching it. It is also the site of glycosylation, where sugar groups are attached to proteins.

12. Why are lysosomes called suicidal bags?

Because they contain hydrolytic enzymes capable of digesting the cell's own components, and their rupture leads to autolysis - self-destruction of the cell. The enzymes work at acidic pH, so even if a few leak into the neutral cytoplasm they are largely inactive, which is a useful safety mechanism.

13. What is the function of the vacuole in a plant cell?

It stores water, ions, pigments and waste products, and it maintains turgor pressure by pressing the cytoplasm against the cell wall. Turgor is what keeps non-woody plants upright, which is why wilting follows water loss. The vacuole can occupy up to 90% of a mature plant cell's volume.

14. What is the function of ribosomes?

Protein synthesis - they are the site where messenger RNA is translated into a polypeptide chain. They are not membrane-bound, which is why prokaryotes have them despite lacking organelles. They may be free in the cytoplasm or attached to the endoplasmic reticulum, depending on the protein's destination.

15. What evidence supports the endosymbiotic theory?

Mitochondria and chloroplasts have their own circular DNA, their own 70S ribosomes resembling those of bacteria, a double membrane, and they divide independently of the cell by a process resembling binary fission. Together these strongly suggest they descend from free-living prokaryotes engulfed by an ancestral eukaryotic cell.

Practice set 3: nucleus and chromosomes

16. Describe the structure of the nucleus.

A double membrane called the nuclear envelope, perforated by nuclear pores, enclosing nucleoplasm that contains chromatin and one or more nucleoli. The outer nuclear membrane is continuous with the rough endoplasmic reticulum. The pores permit selective exchange of RNA and proteins with the cytoplasm.

17. What is the difference between euchromatin and heterochromatin?

Euchromatin is loosely packed, lightly staining and transcriptionally active. Heterochromatin is densely packed, darkly staining and transcriptionally inactive. The distinction reflects accessibility - tightly packed DNA cannot be reached by the transcription machinery, so packing itself regulates gene expression.

18. How are chromosomes classified by centromere position?

Metacentric with the centromere in the middle, giving equal arms; sub-metacentric slightly off-centre, giving one shorter arm; acrocentric near one end, giving one very short arm; and telocentric at the very end, with a single arm. The classification determines the chromosome's shape during anaphase.

19. What is the nucleolus and what does it do?

A dense region within the nucleus, not membrane-bound, where ribosomal RNA is synthesised and ribosomal subunits are assembled. Cells producing large quantities of protein have prominent nucleoli. It disappears during cell division and reforms afterwards, which is itself an examinable detail.

20. What is the function of nuclear pores?

They allow selective two-way transport between nucleus and cytoplasm - messenger RNA and ribosomal subunits move out, while proteins such as histones and polymerases move in. They are not simple holes but complex protein assemblies that regulate what passes, which is what keeps the nuclear and cytoplasmic environments distinct.

Practice set 4: the cell cycle

21. What are the phases of the cell cycle?

Interphase, comprising G1 for growth, S for DNA replication and G2 for preparation, followed by the M phase of division. Interphase occupies well over 90% of the cycle. Cells that stop dividing enter a quiescent G0 stage, which is not part of the active cycle.

22. What are the stages of mitosis and what happens in each?

Prophase, where chromosomes condense and the nuclear envelope breaks down; metaphase, where chromosomes align at the equator; anaphase, where sister chromatids separate to opposite poles; and telophase, where nuclear envelopes reform. Cytokinesis then divides the cytoplasm, producing two genetically identical cells.

23. What is the essential difference between meiosis I and meiosis II?

Meiosis I is the reduction division - homologous chromosomes separate, halving the chromosome number. Meiosis II resembles mitosis, separating sister chromatids without further reduction. Attributing the halving to meiosis II is a common and costly error, since it also misplaces where genetic variation arises.

24. When does crossing over occur and why does it matter?

During prophase I of meiosis, specifically at the pachytene stage, between non-sister chromatids of homologous chromosomes at points called chiasmata. It matters because it recombines maternal and paternal alleles, producing genetic variation - and because recombination frequency is what allows genetic mapping.

25. What is the biological significance of meiosis?

It halves the chromosome number so that fertilisation restores the diploid state rather than doubling it each generation, and it generates variation through crossing over and independent assortment. Both functions are essential to sexual reproduction, and the second is the raw material for natural selection.

26. How do chromosome number and DNA content change through the cell cycle?

DNA content doubles during S phase while the chromosome number stays the same, since each chromosome now has two sister chromatids. The chromosome number itself changes only when chromatids separate at anaphase. Tracking these two quantities separately is exactly what these questions test, and conflating them is the standard error.

Practice set 5: biomolecules and cell function

27. What is the difference between primary and secondary metabolites?

Primary metabolites - amino acids, sugars, nucleotides and lipids - are directly involved in growth and development and are found universally. Secondary metabolites such as alkaloids, pigments, essential oils and toxins have no obvious direct role in basic metabolism but often serve ecological functions such as defence.

28. How do enzymes accelerate reactions?

By lowering the activation energy, providing an active site where substrates are held in the correct orientation. They are highly specific, unchanged by the reaction, and sensitive to temperature and pH because both affect the folded shape on which the active site depends. They alter the rate, never the equilibrium position.

29. What is the cytoskeleton and what does it do?

A network of microtubules, microfilaments and intermediate filaments that gives the cell mechanical support, maintains its shape, and enables movement of organelles and of the cell itself. Microtubules also form the spindle during cell division and the core of cilia and flagella.

30. Which structures demonstrate that mitochondria and chloroplasts are semi-autonomous?

Their own circular DNA, their own 70S ribosomes, a double membrane, and the ability to divide independently of the cell. Semi-autonomous rather than autonomous, because most of their proteins are still encoded by nuclear genes and imported. That partial dependence is exactly what endosymbiotic theory predicts after long coexistence.

How to study this chapter efficiently

  • Study the NCERT diagrams as content, not illustration. Label them from memory - they are examined directly.
  • Build one table of organelles with structure and function. Most questions are a match between the two.
  • Track chromosome number and DNA content separately through the cell cycle. Conflating them causes a whole class of errors.
  • Learn the meiosis I and meiosis II distinction explicitly, including which one halves the chromosome number.
  • Note the 70S ribosome as a shared feature of prokaryotes, mitochondria and chloroplasts. It links three separate topics.
  • Use active recall. This unit has a defined set of retrievable facts, which is precisely the condition where testing beats rereading.

Turn this into active practice

The precision this unit demands is not built by reading. Recognising that lysosomes contain hydrolytic enzymes is easy on the page; producing the stage in which crossing over occurs, under time pressure and among four plausible options, is a different skill.

The NEET Cell Structure quiz on QUFF generates fresh questions across cell types, organelles, the nucleus and the cell cycle, marks them instantly and explains each answer. Do short spaced sets rather than one long session - for a unit of discrete facts, spacing does more for retention than volume.

The bottom line

Now go test yourself

The questions worth rechecking are 3, 15, 23, 24 and 26 - the ribosome sizes, the endosymbiotic evidence, meiosis I as the reduction division, crossing over in prophase I, and tracking DNA content separately from chromosome number. Those five carry the unit's most-tested content.

For final revision, draw and label a generalised eukaryotic cell, then write beside each organelle its single defining function. That one page covers a large share of what this unit asks, and it also prepares the diagram questions directly.

FAQs

Frequently asked questions

When does crossing over occur?

In prophase I of meiosis, at the pachytene stage, between non-sister chromatids of homologous chromosomes. It does not occur in mitosis or in prophase II. It is the main source of genetic recombination and the basis on which genetic maps are constructed.

Which division halves the chromosome number, meiosis I or meiosis II?

Meiosis I. Homologous chromosomes separate there, reducing the number from diploid to haploid. Meiosis II resembles mitosis and separates sister chromatids without further reduction. Attributing the halving to meiosis II also misplaces where variation is generated.

Why are mitochondria and chloroplasts called semi-autonomous?

Because they have their own circular DNA and 70S ribosomes and divide independently of the cell, yet still rely on nuclear genes for most of their proteins. That partial independence is what endosymbiotic theory predicts for organelles descended from engulfed prokaryotes.

Do prokaryotes have any internal structures?

Yes - they have ribosomes, a nucleoid containing the chromosome, and often plasmids and mesosomes. What they lack is membrane-bound organelles. Describing them as structureless is inaccurate and is a distractor NEET uses.

How does DNA content differ from chromosome number during the cell cycle?

DNA content doubles in S phase while the chromosome number stays the same, because each chromosome then has two sister chromatids. The chromosome number changes only when those chromatids separate at anaphase. The two quantities must be tracked independently.

What is the main difference between 70S and 80S ribosomes?

70S ribosomes occur in prokaryotes and inside mitochondria and chloroplasts; 80S ribosomes occur in the eukaryotic cytoplasm. The S values are sedimentation coefficients, which is why subunit values do not add arithmetically - 50S plus 30S gives 70S.

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