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If I try to open one of the files by changing the file extension from.rtf to.txt it opens fine in notepad.

I am going to go ahead and guess that the “.rtf” extension on the MS Word document is the problem. Try copying the document over to your computer and opening it from there with your favorite text editor. It should open fine as plain text.
Another thing to try is using the Save As option on the MS Word document and save it as “.txt” instead.

About a Proof of Regularity of Hypersurfaces in $\mathbb{C}P^n$.

I am reading Chapter V §2, Proposition 3 of the book “Complex Algebraic Surfaces and Holomorphic Mappings” (ed. G. Dethloff, S. Ivashkovich, V. V. Sharko).
The original statement is

Let $H$ be a real hypersurface with singular set $S$ in $\mathbb{C}P^n$.
If $S$ is $n$-dimensional, then $H$ is regular at all points of $S$.

The book gives a proof for $n=1$ and $n=2$.
I am trying to see the proof for $n>2$. In my effort to prove the statement (for $n>2$), I found out some mistakes and cannot find any arguments to make the modified proof correct.
By Proposition 3, since $H$ is real, we have an isomorphism
$$
T_{H^*}^*\vert_H\cong T_H
$$
where $H^*$ is the dual of $H$ and $H$ is viewed as a complex hypersurface in $\mathbb{C}P^n$.
Moreover, since $\mathbb{C}P^n$ is Hermitian symmetric,
$$
T_{H^*}^*\vert_H\cong i\,T_H\cong i\, T_{\mathbb{C}P^n}(H)\cong i\, T_{\mathbb{C}P^n}|_H\cong T_H(T_{\mathbb{C}P^n}|_H)\cong T_H(T

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Primary Bond Removal From Hydrogen-Bonded Systems. Part II: Application to Characteristic Features of the Arrhenius Reaction.
The dynamic of a local minimum (LM) state of a molecular hydrogen-bonded system is investigated using perturbation theory within the restricted molecular orbital (RMO) framework. The vibrational mode of interest is one which does not break a local hydrogen bond but does change the orientation of an individual hydrogen bond relative to the local potential energy surface of the LM state. The results indicate that the rate constant for exchange of the hydrogen bond from the LM state to a different, higher state may be obtained by a rate-limiting vibrational mechanism of the mode of interest. The predictions are compared with a previous estimate of this rate obtained by a different, but related, theoretical methodology. This comparison indicates that the inclusion of the “Cabrera effect” with the method of Finer et al. [ J. Chem. Phys. 108, 10608 (1998)] is necessary to obtain reliable estimates of the rate of hydrogen bond reorientation. The results have implications for the interpretation of vibrational spectra of hydrogen-bonded systems.Determination of 5alpha-cholest-8(14)-en-3beta-ol in rat plasma by high-performance liquid chromatography with precolumn derivatization.
A high-performance liquid chromatographic (HPLC) method has been developed for the determination of 5alpha-cholest-8(14)-en-3beta-ol in rat plasma using [14C]5alpha-cholest-8(14)-en-3beta-ol as an internal standard. After addition of the internal standard and extraction with n-hexane:2-propanol (50:50, v/v), the extract was concentrated to dryness and the residue was applied to a Sep-Pak C18 cartridge. The cartridge was washed with ethyl acetate, and the butyl ether eluate was injected into the HPLC system. The chromatography was carried out isocratically on a C18 reversed-phase column with hept