CUET · PHYSICS · PYQ PAPER 2025
When a potential difference is applied across a copper wire, the drift velocity of the electrons is v. If the same potential difference is applied across another copper wire of the same length but twice the diameter, the drift velocity of electrons will be
- A 2v
- B 3v
- C v
- D v/2
Answer & Solution
Correct Answer
(C) v
Step-by-step Solution
Detailed explanation
\( v_d = \frac{V}{ne\rho L} \) Since \(V\), \(n\), \(e\), \(\rho\), and \(L\) are constant, \(v_d\) is independent of diameter. The drift velocity will be \(v\).
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Choose the correct answer from the option given below :CUET 2025 Medium - Read the passage given below and answer the question.
The transition elements which give the greatest number of oxidation states occur in or near the middle of the series. Manganese, for example, exhibits all the oxidation states from +2 to +7 . The lesser number of oxidation states at extreme ends stems from either too few electrons to lose or share (Sc, Ti) on too many d-electrons (hence fewer orbitals available in which to share electrons with others) for higher valence \(( Cu , Zn )\). Thus early in the series scandium (II) is virtually unknown and titanium (IV) is more stable than Ti (III) or Ti (II). At the other end, the only oxidation state of zinc is \(+ 2\) (no d electrons are involved). The maximum oxidation states of reasonable stability correspond in value to the sum of the s - and d-electrons upto manganese ( \(Ti ^{I V} O _2, V^V O _2^{+}, Cr ^{V I} O _4^{2-}\), \(Mn ^{\text {VII }} O _4\) ) followed by a rather abrupt decrease in stability of higher oxidation states, so that the typical species to follow are \(Fe ^{I I, I I I}, Co ^{I I, I I I}, Ni ^{I I}, Cu ^{I, I I}, Zn ^{I I}\).
The variability of oxidation states, a characteristic of transition elements, arises out of incomplete filling of d-orbitals in such a way that their oxidation states differ from each other by unity, e.g. \(V ^{I I}, V^{I I I}, V^{I V}, V^V\). This is in contrast with the variability of oxidation states of non transition elements where oxidation states normally differ by a unit of two.
An interesting feature in the variability of oxidation states of the d-block elements is noticed among the groups (groups 4 through 10). Although in the p-block, the lower oxidation states are favoured by the heavier members (due to inert pair effect), the opposite is true in the groups of dblock. For example, in group 6, \(Mo ( VI )\) and \(W ( VI )\) are found to be more stable than \(Cr ( VI )\). The \(Cr ( VI )\) in the form of dichromate in acidic medium is a strong oxidising agent, whereas \(MoO _3\) and \(WO _3\) are not.
Low oxidation states are found when a complex compound has ligands capable of \(\pi\)-acceptor character in addition to the \(\sigma\)-bonding. For example, in \(Ni ( CO )_4\) and \(Fe ( CO )_5\), the oxidation state of nickel and iron is zero.
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