AP Biology Unit 5: Heredity

Unit 5 covers heredity: Mendelian inheritance, non-Mendelian patterns, chromosomal inheritance and meiosis. The exam favours reasoning from a pedigree or a cross over reciting ratios.

157 questions7 CED topics69% with a figure
How this unit behaves

What 157 questions on it look like

69% of the questions come with a figure — a graph, diagram or data display. Reading the figure correctly is most of the work before any content knowledge applies.

Non-Mendelian Genetics53
Chromosomal Inheritance37
Mendelian Genetics22
Environmental Effects on Phenotype18
Meiosis and Genetic Diversity18
Meiosis6
Non-Mendelian Genetics and Independent Assortment3

Questions per CED topic.

From the bank

Three real heredity questions

Drawn from the practice pool, not from the mock papers.

Mendelian Genetics · Statistical Tests and Data Analysis · with figure

A dihybrid cross is expected to produce a 9:3:3:1 phenotype ratio. The observed counts for 160 offspring are shown. What is the approximate chi-square value?

  1. A1.20; only the third class contribution
  2. B0.18; only the first class contribution approximated
  3. C3.84; a common critical value, not this statistic
  4. D4.98; the sum of all four chi-square termscorrect
Why D is correct

Expected counts are 90, 30, 30, and 10. Chi-square = 4/90 + 4/30 + 36/30 + 36/10 = approximately 4.98.

The stem asks for a numerical or quantitative judgment: "A dihybrid cross is expected to produce a 9:3:3:1 phenotype ratio. The observed counts for 160 offspring are...". The safe route is to identify the counted event, use the full denominator, and then interpret the number biologically. Here the worked reasoning is Expected counts are 90, 30, 30, and 10, so choices based on 1.20; only the third class contribution or 0.18; only the first class contribution approximated lose the required setup.

Common mistakes. Do not stop at a nearby term such as 1.20; only the third class contribution or 0.18; only the first class contribution approximated. The explanation has to make "4.98; the sum of all four chi-square terms" fit this stem clue: "A dihybrid cross is expected to produce a 9:3:3:1 phenotype ratio. The observed counts...".

Non-Mendelian Genetics and Independent Assortment · Statistical Tests and Data Analysis · with figure

In a testcross for two linked genes, the offspring counts are shown. What is the approximate recombination frequency?

  1. A5.9%; using only recombinant type 2
  2. B12%; using both recombinant classes out of all offspringcorrect
  3. C44%; using one parental class as the numerator
  4. D6.1%; using only recombinant type 1
Why B is correct

Recombinant offspring total 61 + 59 = 120 out of 1000 total offspring. The recombination frequency is 120/1000 x 100% = 12%.

The stem asks for a numerical or quantitative judgment: "In a testcross for two linked genes, the offspring counts are shown. What is the approximate recombination frequency". The safe route is to identify the counted event, use the full denominator, and then interpret the number biologically. Here the worked reasoning is Recombinant offspring total 61 + 59 = 120 out of 1000 total offspring, so choices based on 5.9%; using only recombinant type 2 or 44%; using one parental class as the numerator lose the required setup.

Common mistakes. Do not stop at a nearby term such as 5.9%; using only recombinant type 2 or 44%; using one parental class as the numerator. The explanation has to make "12%; using both recombinant classes out of all offspring" fit this stem clue: "In a testcross for two linked genes, the offspring counts are shown. What is the...".

Chromosomal Inheritance · Statistical Tests and Data Analysis

A recessive X-linked allele causes a trait. A carrier female and an unaffected male have a son. What is the probability that the son will express the trait?

  1. A1/4; the probability from an autosomal carrier cross
  2. B3/4; the probability of not expressing the trait in some autosomal crosses
  3. C1/2; the son receives one of the mother's two X chromosomescorrect
  4. D0; a carrier mother cannot pass the allele to a son
Why C is correct

A son receives his X chromosome from his mother and Y chromosome from his father. A carrier mother has a 1/2 chance of passing the recessive X-linked allele to a son.

The stem asks for a numerical or quantitative judgment: "A recessive X-linked allele causes a trait. A carrier female and an unaffected male have a son. What is the...". The safe route is to identify the counted event, use the full denominator, and then interpret the number biologically. Here the worked reasoning is A carrier mother has a 1/2 chance of passing the recessive X-linked allele to a son, so choices based on 1/4; the probability from an autosomal carrier cross or 3/4; the probability of not expressing the trait in some autosomal... lose the required setup.

Common mistakes. Do not stop at a nearby term such as 1/4; the probability from an autosomal carrier cross or 3/4; the probability of not expressing the trait in some autosomal.... The explanation has to make "1/2; the son receives one of the mother's two X chromosomes" fit this stem clue: "A recessive X-linked allele causes a trait. A carrier female and an unaffected male have...".

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FAQ

Heredity questions

What genetics maths do I need?

Punnett squares, the product and sum rules, and chi-square. The arithmetic is light; the interpretation is what is tested.

How do I read a pedigree quickly?

Look for an affected child with unaffected parents — that establishes recessive — then check whether affected individuals are disproportionately male.
Last reviewed 2026-08-28. Unit and topic names follow the College Board course framework. Question counts describe the PrepScore practice bank, not the exam.
Topic by topic

Worked questions by topic

4 of this unit’s topics have enough practice questions for a page of their own.

Practise heredity until the reasoning is automatic.

Real AP questions with a full explanation on every answer, and a mistake bank that only clears when you get it right.