A film projector and microscope give equal magnification. But a film projector is not used to see living cells because
a microscope has greater resolving power than a projector.
The question asks why a film projector, despite having the same magnification as a microscope, is unsuitable for viewing living cells.
Magnification makes objects appear larger, while resolving power determines the ability to distinguish between two closely spaced points. Both are important for viewing small objects, but resolving power is critical for seeing detail.
A film projector magnifies an existing image (from a film frame) to be viewed on a large screen. Its primary function is magnification for distant viewing, not the resolution of minute details inherent in the original image subject (like a cell).
The key difference lies in resolving power. Microscopes possess significantly higher resolving power compared to film projectors. While both might magnify equally, only the microscope can distinguish the fine details necessary to observe the structures within living cells.
Therefore, a film projector is not used to see living cells because a microscope has greater resolving power, enabling the visualization of the fine details essential for cell observation.
A monochromatic and linearly polarised light is used in a Young's double slit experiment. A linear polarizer, whose pass axis is at an angle $45^\circ$ to the polarization of the incident wave, is placed in front of one of the slits. If $I_{max}$ and $I_{min}$, respectively, denote the maximum and minimum intensities of the interference pattern on the screen, the visibility, defined as the ratio $\frac{I_{max} - I_{min}}{I_{max} + I_{min}}$ is
A screen has two slits, each of width $w$, with their centres at a distance $2w$ apart. It is illuminated by a monochromatic plane wave travelling along the $x$-axis.

The intensity of the interference pattern, measured on a distant screen, at an angle $\theta = n\lambda/w$ to the $x$-axis is
A pair of parallel glass plates separated by a distance $d$ is illuminated by white light as shown in the figure below. Also shown is the graph of the intensity of the reflected light $I$ as a function of the wavelength $\lambda$ recorded by a spectrometer.
Assuming that the interference takes place only between light reflected by the bottom surface of the top plate and the top surface of bottom plate, the distance $d$ is closest to