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A coupling of probability distributions $\mu ,\nu$ is a joint probability distribution of random variables $(X,Y)$ whose marginal distributions are $\mu ,\nu$. It lets us choose the statistical dependence between two random constructions while preserving the individual laws. This choice can make a comparison much easier: giving two simulations the same random input may keep their paths close, even though separately generating both paths would hide that relationship.^[ref]

For example, two fair coin tosses can be generated independently, with mismatch probability $1/2$, or by tossing once and setting $Y=X$, with mismatch probability zero. Both constructions have the same two Bernoulli distributions as marginals. Their joint laws differ. A maximal coupling makes the values agree as often as possible; a coalescing coupling arranges permanent agreement of two processes after a random time. Minimizing expected geometric separation instead leads to Wasserstein distance.

For any coupling of random variables, the coupling characterization of total variation distance gives $d_{\mathrm{TV}}(\mathcal{L}(X),\mathcal{L}(Y))\le \mathbb{P}(X\ne Y)$, where $\mathcal{L}$ denotes the law of a random variable. If two coupled Markov chains stay identical after their coalescence time $T$, then $\{X_t\ne Y_t\}\subseteq \{T>t\}$ andThe persistent agreement is essential: a first meeting time does not give this bound if the chains can separate again. A coalescing coupling turns a difficult comparison of probability distributions into a concrete question about how long a joint simulation takes to merge.

Suppose an involution $R$ of a Markov chain satisfies $P(Rx,Ry)=P(x,y)$. Start one chain at $x$, set the other equal to its image under $R$ until the first hitting time of the fixed-point set of $R$, and subsequently use identical transitions. This is a coalescing coupling, because the symmetry preserves each marginal transition matrix and both chains coincide at that hitting time.

Let $R$ interchange the two complete graphs, sending $v_i$ to $v_i^{\prime }$ and fixing $w$. This involution preserves the transition matrix of the simple random walk. A mirror coupling under an involution starts $X$ at $v_i$, keeps $Y_t=R(X_t)$ until the hitting time $\tau$ of $w$, and then makes the two walks move identically. Each coordinate has the correct transition probabilities, and they coalesce precisely at $\tau$. The coupling inequality for total variation gives

There is a genuine error in the printed expected hitting time bound, as well as an unspecified initial law. For $n\ge 2$, write $a={\mathbb{E}}_{v_1}\tau$ and $b={\mathbb{E}}_{v_i}\tau$ for $i\ne 1$. From every clique vertex there is a positive chance of reaching $w$ within two steps, uniformly over the finite state space for each fixed $n$, so $\tau$ has finite expected value. First-step analysis, using the degree of a vertex $n$ at $v_1$ and $n-1$ at the other clique vertices, givesSolving these linear equations yieldsIn particular even the attachment vertex exceeds the printed bound by one. The valid uniform replacement is ${\max }_x{\mathbb{E}}_x\tau \le n^2$, the hitting time of the bridge vertex between two cliques formula.

We must also handle arbitrary starting states, including $w$, before applying the mirror argument. Identify related vertices and consider the lumped Markov chain $Z$ on $\{1,\dots ,n,w\}$. Its transition matrix $Q$ has $Q(1,j)=1/n$ for $j\ne 1$, $Q(1,w)=1/n$, $Q(i,j)=1/(n-1)$ for $i\ne 1$ and $j\ne i$, and $Q(w,1)=1$, with all other entries zero. Here the row for $i\ne 1$ only ranges over $j\in \{1,\dots ,n\}$.

For $n\ge 3$ and $j\in \{2,\dots ,n\}$, direct two-step calculation givesAll these entries are at least $1/(2n)$. Thus $Q^2(z,\cdot )\ge \alpha \nu (\cdot )$ for every $z$, where $\nu$ is the uniform distribution on a finite set $\{2,\dots ,n\}$ and $\alpha =(n-1)/(2n)\ge 1/3$. This is a Doeblin condition. At each two-step block couple the two quotient endpoints to the same sample from $\nu$ with probability $\alpha$, using the residual probability distributions otherwise. The first successful block has expected value at most $1/\alpha$, so the alignment time $A$ has $\mathbb{E}A\le 6$. Lift each endpoint coupling of probability distributions to the original walks by their conditional two-step path laws; this preserves every marginal path law. The success test uses fresh block randomness and so permits restarting the walks with their original transition matrix at the aligned endpoints.

At alignment the original walks are equal or related. Use identical transitions in the first case and the mirror coupling under an involution in the second. The resulting coalescing coupling has coalescence time $T$ satisfying $\mathbb{E}T\le 6+n^2$ for every pair of initial states. Therefore Markov inequality and the pairwise mixing diameter implyFor the hint's particular starting states, the quotient one-step laws from two different clique indices have a common component of mass at least $1-2/n$: for two ordinary indices it is $(n-2)/(n-1)$; for one attachment index it is $(n-2)/n$. A maximal coupling therefore aligns those indices with probability $1-O(1/n)$, as suggested. The two-step argument above additionally covers $w$.

The nonlazy walk is an aperiodic Markov chain for $n\ge 3$, because the connected graph contains a triangle. For $n=1,2$ it is a periodic Markov chain on a bipartite graph; each bipartition class has stationary mass $1/2$, and the walk stays on a single class at each time. Hence $d(t)\ge 1/2$ and the $1/4$ mixing time is infinite. The asymptotic conclusion is valid for $n\ge 3$.