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Adachi I, T Masuda, and S Nushiyama, ATesting of Optical Materials by the Twyman Type Interferometer, Atti Fond Giorgio Ronchi Contrib Ist Naz Ottica, 16, 666 (1961) Adachi I, T Masuda, T Nakata, and S Nushiyama, The Testing of Optical Materials by the Twyman Type Interferometer III, Atti Fond Giorgio Ronchi Contrib Ist Naz Ottica, 17, 319 (1962) Balhorn R, H Kunzmann, and F Lewosky, Frequency Stabilization of Internal Helium-Neon Lasers, Appl Opt, 11, 742 (1972) Basile G, Two-Wave Interferometers for Use with a Monochromatic Source, Appl Opt, 18, 422, (1979) Batishko C R and R R Shannon, Problem in Large-Path Difference Laser Interferometry; Appl Opt, 11, 195 (1972) Bennett S J, R E Ward, and D C Wilson, Comments on Frequency Stabilization of Internal Mirror He-Ne Lasers, Appl Opt, 12, 1406 (1973) Berggren R, Analysis of Interferograms, Opt Spectra.



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Because reentering the starting point is difficult, and the contents of the floating box will appear to jump if you don t get it exact, I recommend getting position 2 first, and then position 1.

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, 4, 22 (1970) Birch K G, Oblique Incidence Interferometry Applied to Non-Optical Surfaces, J Phys E, 6, 1045 (1973) Birch K G, Interferometric Examination of Lenses and Other Components, Proc SPIE, 163, 112, (1979) Briers J D, Interferometric Testing of Optical Systems and Components: A Review, Opt Laser Technol, 4, 28 (1972) Bruning J and D R Herriott, A Versatile Laser Interferometer, Appl Opt, 9, 2180 (1970) Bruning J H, D R Herriott, J E Gallagher, D P Rosenfeld, A D White and D J Brangaceio, Digital Wavefront Measuring Interferometer for Testing Surfaces and Lenses, Appl Opt 13, 2693 2703 (1974) Buin A P, M P Semenova, and Kriuyukhina, Inspection of the Surface Quality of Large Scale Optical Components of an Unequal Arm Interferometer, Sov J Opt Technol, 36, 720 (1969) Burch C R, The Williams Interferometer, Monthly Not.

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very low lying and polarized away from C, one can legitimately regard the -CF3 group as a Z-type substituent 2 Use orbital interaction analysis to explain stabilization of a carbocationic center by a cyclopropyl group What kind of substituent (X:, ``C,'' or Z) is cyclopropyl Explain Predict the orientation of the planar cationic center relative to the cyclopropyl ring 3 By considering the p MOs of the cyclopentadienyl system (C5 H5 ) to result from an interaction between cis-butadiene p MOs and an sp 2 hybridized C atom, explain the stability of the cyclopentadienyl anion and the instability of the cyclopentadienyl cation 4 Use simple orbital interaction arguments (ie.

, orbital correlation diagrams) to explain the following: (a) Stabilization of a carbocation by C H hyperconjugation (b) Stabilization of a carbanion by C F negative hyperconjugation (c) Triplet ground state of phenyl carbene, C6 H5 C H (d) Singlet nature of cycloheptatrienylidene, (e) Nucleophilicity of N,N-dimethylaminocarbinyl radical, (CH3 )2 NCH2 Answer to 4(d) We can consider the orbitals of cycloheptatrienylidene to arise from the interaction of the p orbitals of hexatriene and the valence orbitals of a dicoordinated carbon atom (a 2p orbital and an sp n hybrid orbital) The p orbitals of hexatriene may be obtained from an SHMO calculation The interaction diagram is shown in Figure B72 The p orbital of the carbene site is raised as a result of the dominant interaction with p3 of hexatriene.

R Soc, 100, 488 (1940) Candler C, Modern Interferometers, Hilger and Watts, London, 1951, Chaps 6 and 7 Chen C W and J B Breckinridge, Holographic Twyman Green Interferometer, Appl Opt, 21, 25-63 (1982) Cole G C, J H Burge, and L R Dettmann, Vibration Stabilization of a Phase Shifting Interferometer for Large Optics, Proc SPIE, 3134, 438 446 (1997) Collier R T, C B Brukhardt, and L H Lin, Optical Holography, Academic Press, New York, 1971, p 146..

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