← Openai Interview Insights

Openai·Software Engineer·Technical Phone Screen·Senior

SeniorPrefer not to say
May 2026

Summary

OpenAI SWE coding round built around a single cellular automaton problem that expands across five increasingly brutal sub-parts. The core pattern is multi-source BFS on a grid, but the later parts layer in per-cell state tracking that breaks the clean BFS skeleton. Passing bar is reportedly finishing the first three parts cleanly within the hour.

Questions Asked (5)

Q1

Given an M×N grid with some initially infected cells and the rest healthy, simulate infection spreading to all 4-directional neighbors simultaneously each day. Return the number of days until every cell is infected, or -1 if full infection is impossible.

Algorithms & Data Structures
Author's notes

This is basically rotting oranges with a coat of paint.

Create a free account to read the full note

AI HintsAI Generated

Suggested Approach

Model the grid as a graph and use multi-source BFS starting from all initially infected cells simultaneously. Track the number of days (BFS levels) until no more cells can be infected, then check if all cells are infected; if not, return -1.

Pro tip: Clarify edge cases upfront, such as an empty grid or no initially infected cells, and discuss time/space complexity (O(M*N)) to demonstrate thoroughness.

1. Understand the problem and edge cases

Confirm the grid dimensions, infection spread rules, and what constitutes a 'day'. Discuss edge cases like empty grid, all cells initially infected, or no initially infected cells.

2. Choose the right algorithm

Recognize that simultaneous spread from multiple sources is naturally handled by multi-source BFS. Explain why BFS is optimal for finding the minimum time to reach all cells.

3. Implement multi-source BFS

Initialize a queue with all initially infected cells and set their distance to 0. Process level by level, infecting healthy neighbors and incrementing the day count after each level.

4. Track and return the result

After BFS, check if any healthy cells remain. If yes, return -1; otherwise, return the number of days (max distance from any source).

5. Analyze complexity and test

State that time and space complexity are O(M*N). Walk through a small example to verify correctness and discuss potential optimizations.

Key Points to Mention

  • Multi-source BFS to simulate simultaneous infection spread
  • Time and space complexity: O(M*N)
  • Handling edge cases: empty grid, no initial infection, all infected
  • Using a queue to process cells level by level (each level = one day)
  • Checking for uninfected cells after BFS to return -1 if needed
  • Avoiding unnecessary re-processing of infected cells

AI-generated suggestions, not part of the candidate's original notes. May be inaccurate — verify before relying on them.

Q2

Extend the infection simulation to include immune cells that can never be infected and never propagate. Return days until all reachable healthy cells are infected, or -1 if any healthy cell is permanently walled off by immune cells.

Algorithms & Data Structures
Author's notes

Cleaner than it sounds once you realize immune cells are just walls.

Create a free account to read the full note

AI HintsAI Generated

Suggested Approach

Model the grid as a graph and run a multi-source BFS from all initially infected cells, treating immune cells as blocked. After BFS, check if any healthy cell remains unvisited; if so, return -1, otherwise return the maximum distance reached.

Pro tip: Clarify edge cases upfront: what if there are no healthy cells initially? What if immune cells completely isolate a region? Also, mention that you can optimize by tracking the count of infected cells to early-exit if all reachable cells are infected.

1. Clarify problem constraints and edge cases

Ask about grid size, movement directions (4 or 8), and whether immune cells are static. Confirm that 'reachable' means via 4-directional adjacency and that immune cells block infection.

2. Model as graph and choose algorithm

Represent each cell as a node; edges connect adjacent non-immune cells. Use multi-source BFS from all initially infected cells to compute the minimum time to infect each healthy cell.

3. Implement BFS with distance tracking

Initialize a queue with all infected cells at day 0. While queue is not empty, pop a cell, and for each non-immune, uninfected neighbor, mark infected, set distance = current distance + 1, and enqueue. Track the maximum distance.

4. Check for unreachable healthy cells

After BFS, iterate through all cells. If any healthy cell remains uninfected, return -1. Otherwise, return the maximum distance recorded.

5. Analyze complexity and potential optimizations

Time complexity is O(N*M) since each cell is processed once. Space is O(N*M) for the queue and visited set. Mention early termination if all healthy cells are infected before BFS completes.

Key Points to Mention

  • Multi-source BFS to simulate simultaneous infection spread
  • Immune cells act as obstacles and are never infected
  • Track maximum distance to determine days until all reachable cells are infected
  • Post-BFS check for any remaining healthy cells to return -1
  • Time and space complexity: O(N*M) for an N x M grid
  • Edge cases: no healthy cells, all cells immune, disconnected components

AI-generated suggestions, not part of the candidate's original notes. May be inaccurate — verify before relying on them.

Q3

Add a recovery mechanic: after being infected for D days, a cell becomes permanently immune and stops spreading. Return the number of days until no active infections remain anywhere in the grid.

Algorithms & Data StructuresTechnical Trade-offs
Author's notes

This is where things get genuinely annoying.

Create a free account to read the full note

AI HintsAI Generated

Suggested Approach

Model the infection and recovery using a multi-source BFS where each cell tracks its infection start day, and when a cell reaches D days infected, it becomes immune and stops spreading. Simulate day by day, updating states and counting active infections until none remain, returning the total days elapsed.

Pro tip: Clarify upfront whether D is inclusive (e.g., infected for D days means it recovers at the start of day D+1) and whether immunity is permanent; this avoids off-by-one errors and shows attention to detail.

1. Clarify rules and edge cases

Confirm the meaning of 'infected for D days', whether recovery happens at the start or end of a day, and if immunity is permanent. Also discuss grid boundaries, initial infected cells, and whether multiple waves can occur.

2. Choose data structures

Use a queue for BFS to process newly infected cells, a 2D array to track each cell's state (healthy, infected, immune) and infection start day, and a counter for active infections.

3. Simulate day by day

For each day, first process recoveries: any cell infected for D days becomes immune and is removed from active infections. Then spread infection from currently infected cells to healthy neighbors, updating their state and start day.

4. Track and return days

Increment a day counter each simulation step, and stop when the active infection count reaches zero. Return the total days elapsed.

5. Analyze complexity and trade-offs

Discuss time complexity O(N*M) where N and M are grid dimensions, and space complexity O(N*M). Mention alternative approaches like event-driven simulation if D is large, and trade-offs between clarity and efficiency.

Key Points to Mention

  • Multi-source BFS to simulate simultaneous spread from all initially infected cells.
  • Tracking infection start day per cell to determine when D days have passed.
  • State transitions: healthy -> infected -> immune, with immune cells never spreading again.
  • Day-by-day simulation with a queue for efficient processing of newly infected cells.
  • Handling edge cases: no initial infections, D=0, grid boundaries, and multiple disconnected regions.
  • Time and space complexity analysis, and potential optimizations for large grids or large D.

AI-generated suggestions, not part of the candidate's original notes. May be inaccurate — verify before relying on them.

Q4

Further extend the simulation with threshold-based infection: a healthy cell only becomes infected if it has at least K infected neighbors. Alternatively, add a death mechanic where infected cells with K or more infected neighbors begin a death countdown. Return relevant counts or timings depending on the variant.

Algorithms & Data StructuresTechnical Trade-offs
Author's notes

Didn't get here personally but from what I've heard there are at least three different versions of this part floating around depending on who's running your loop.

Create a free account to read the full note

AI HintsAI Generated

Suggested Approach

Clarify the variant (threshold infection or death countdown) and define the grid and neighbor rules. Then outline a simulation loop that tracks state changes and counts, using appropriate data structures for efficiency. Finally, discuss how to return the required counts or timings and analyze trade-offs.

Pro tip: Demonstrate awareness of performance by suggesting optimizations like using a queue for active cells or parallelizing updates, and mention edge cases such as K=0 or K greater than the number of neighbors.

1. Clarify requirements and assumptions

Ask clarifying questions about grid size, neighbor definition (e.g., Moore or von Neumann), K value, and whether multiple variants should be supported. Confirm what counts or timings need to be returned.

2. Design the simulation model

Define cell states (healthy, infected, dead) and transition rules. For threshold infection, a healthy cell becomes infected if infected neighbors >= K. For death countdown, infected cells with infected neighbors >= K start a countdown and die after a set number of steps.

3. Choose data structures and algorithm

Use a 2D array for the grid and maintain counts of infected neighbors, possibly with a secondary array. For efficiency, consider updating only cells whose neighbor counts change, using a queue or set of active cells.

4. Implement simulation loop and track metrics

Iterate over time steps, applying rules simultaneously (using a copy or double buffer). Track relevant metrics such as total infected over time, time to reach steady state, or number of deaths per step.

5. Return results and discuss trade-offs

Return the required counts or timings based on the variant. Discuss time/space complexity and potential optimizations, and mention how the approach scales with grid size and K.

Key Points to Mention

  • Simultaneous updates: use double buffering or a copy of the grid to avoid order-dependent artifacts.
  • Neighbor counting: efficiently compute infected neighbor counts, possibly using convolution or incremental updates.
  • Threshold logic: handle edge cases like K=0 (always infect) or K > max neighbors (never infect).
  • Death countdown: maintain a separate countdown timer per infected cell, decrementing each step when condition holds.
  • Termination conditions: define when simulation stops (e.g., no state changes, max steps, or all cells dead).
  • Complexity analysis: O(N*M) per step for naive approach, but optimizations can reduce to O(active cells).

AI-generated suggestions, not part of the candidate's original notes. May be inaccurate — verify before relying on them.

Q5

Each day you can choose one row or column and eliminate all cells in it. Design a strategy to minimize total deaths across the grid.

Algorithms & Data Structures
Author's notes

Almost nobody gets here.

Create a free account to read the full note

AI HintsAI Generated

Suggested Approach

First, clarify the problem: the grid has cells with death counts, and each day you choose a row or column to eliminate all remaining cells in it. The goal is to minimize total deaths. This is a combinatorial optimization problem; likely NP-hard, so discuss greedy strategies, dynamic programming for small grids, or integer programming formulations. Also consider if the grid is fully known and if choices are adaptive.

Pro tip: Show awareness that this is a variant of the maximum coverage problem or set packing, and that a greedy heuristic (e.g., pick the row/column with the highest sum of remaining deaths) often performs well but may not be optimal. Mention that for small grids, you can solve it exactly with DP over subsets of rows/columns.

1. Clarify the problem

Ask about the grid size, whether death counts are known in advance, and if choices are adaptive. Confirm that eliminating a row/column removes all remaining cells in it, and that the goal is to minimize total deaths.

2. Identify problem class

Recognize this as a combinatorial optimization problem similar to maximum coverage or set packing. Note that it is likely NP-hard, so exact solutions may be infeasible for large grids.

3. Propose exact solution for small grids

For small grids (e.g., up to 20 rows/columns), use dynamic programming over subsets of rows and columns, or integer programming, to find the optimal sequence.

4. Propose heuristic for large grids

For large grids, suggest a greedy heuristic: repeatedly choose the row or column with the highest sum of remaining deaths. Discuss its approximation ratio and potential improvements like local search.

5. Analyze and compare

Compare the greedy approach to other heuristics (e.g., random, simulated annealing) and discuss trade-offs between optimality and computational efficiency. Mention that the greedy approach is simple and often effective.

Key Points to Mention

  • NP-hardness and relation to maximum coverage/set packing
  • Dynamic programming over subsets for exact solution on small grids
  • Greedy heuristic: pick row/column with maximum remaining sum
  • Approximation ratio of greedy (e.g., 1-1/e for submodular maximization)
  • Integer programming formulation for exact solution
  • Adaptive vs non-adaptive strategies and their impact

AI-generated suggestions, not part of the candidate's original notes. May be inaccurate — verify before relying on them.