You can google the substances themselves. Then there are lots of tables. Here is one specifically referring to your question.
http://www.chemrat.com/ChemHog2/Organic Chem_files/pKtrends.doc. You have to know what pK means, but it you haven't done it, it suffices that it is the pH at which the acid is half-dissociated. But then you have to know what pH means.
So we'd class H
2Se as a weakish acid a bit more acidic than acetic. H
2Te is getting to be strongish. This may be the first and last time you meet it. And even H
2Se not often. The real thing you're likely to met later is that H
2S is a weak acid as are very many common RSH ((sulphydryl aka thiols aka mercaptans) which include important biological molecules like the amino acid cysteine. Their dissociation occurs over the neutral or physiological range, pK's round 6.75 - 8. Weak acids but much stronger than the corresponding alcohols.
If the rationalisations you are expected to learn about factors of acid strength make sense, OK, whenever they don't, don't worry, because the ones that have got fossilised in textbooks are all inadequate less-than-half truths that leave out the fundamental role of the solvent.