221 Microsoft Word Shortcuts 1 Ctrl + Shift + A All Caps Makes the selection all capitals (toggle) 2 Alt + Ctrl + 1 Apply Heading1 Applies Heading 1 style to the selected text 3 Alt + Ctrl + 2 Apply Heading2 Applies Heading 2 style to the selected text 4 Alt + Ctrl + 3 Apply Heading3 Applies Heading 3 style to the selected text 5 Ctrl + Shift + L Apply List Bullet Applies List Bullet style to the selected text 6 Alt + F10 App Maximize Enlarges the application
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six-week schedule there were significant open shifts and not enough staff to cover all the open shifts. The objectives for the project were to calculate the new (ADC)‚ and to recalculate‚ in decimals‚ the core staffing needs for an 8-hour shift‚ for each shift in every inpatient nursing unit. The new calculations would then be entered into the staffing configurations of the staffing and scheduling program. The goal was to close the gap on open shifts at the start of the schedule‚ thus eliminating
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Ctrl References click left button double click left button click right button Mouse X2 to connect a Group with a Joint. Hold SHIFT and click left mouse button Shift to disconnect a Group from a Joint. SHIFT + Double click to disconnect Quick Reference Card X2 Shift Corkscrew Joint Spring Joint Ball Joint Universal Joint Shift hold shift button hold ctrl button all from object/joint Sketchy Solids Toolbar Create a Box Create a Sphere Ctrl to change its centering
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The Right Shift Theory In 1972‚ Marian Annett of the University of Leicester UK proposed a theory that came to be known as the Right Shift Theory. She believed that as humans evolved‚ all of the major functions of the brain‚ such as speech‚ shifted to being controlled and centered in the left hemisphere of the brain‚ which controls the right side of the body naturally. By shifting important functions to the left‚ a bias for the right hand would be created. This lateralization and biased‚ according
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Chinh Minh Le Due date: 09/17/2013 Operation date: 09/16/2013 Class: ITCS 3181‚L Fall 2013 I. Purpose: The goal of this assignment is to design a 4-bit expandable shifter. Input two 4-bit D3D2D1D0‚ output is shift of inputs. They depend on right shift or left shift or non shift. All of things‚ we should begin from smallest elements‚ then after we develop it. So‚ in this assignment‚ I begin from smallest elements such as: XOR‚ 2-in AND‚ 2-in OR‚ and NOT gates. I take ownership of these components
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Published on Web 05/25/2006 A Solid-State 95Mo NMR and Computational Investigation of Dodecahedral and Square Antiprismatic Octacyanomolybdate(IV) Anions: Is the Point-Charge Approximation an Accurate Probe of Local Symmetry? Michelle A. M. Forgeron and Roderick E. Wasylishen* Contribution from the Department of Chemistry‚ Gunning/Lemieux Chemistry Centre‚ UniVersity of Alberta‚ Edmonton‚ Alberta‚ Canada T6G 2G2 Received January 6‚ 2006; Revised Manuscript Received April 6‚ 2006; E-mail:
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because even though it got really busy when 10 Japanese customers came in at the same time one night‚ she rushed through and was able to satisfy the customers’ needs. It is not fair to Cindie that she has to close up by herself and often work the late shift just because she is the “new kid on the block” (Mintz & Morris‚ 2011). Everybody should be treated equally (Mintz & Morris‚ 2011). From the perspective of Kohlberg’s six stages of moral development‚ Cindie could report Lyndell’s behavior to the store
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The Grignard Synthesis of Triphenylmethanol Organic Chemistry Lab II March 19‚ 2012 Abstract The purpose of this experiment was to synthesize the Grignard reagent‚ phenyl magnesium bromide‚ and then use the manufactured Grignard reagent to synthesize the alcohol‚ triphenylmethanol‚ by reacting with benzophenone and protonation by H3O+. The triphenylmethanol was purified by recrystallization. The melting point‚ Infrared Spectroscopy‚ 13C NMR‚ and 1H NMR were used to characterize and confirm
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Abstract:The Wittig Reaction is a nucleophilic addition in which an alkene is formed as a product. Both the E and Z isomers of the alkene result. Substituents on the aromatic aldehyde affect the E/Z ratio of products that form. In this experiment‚ a nitro group was used as the substituent in the ortho‚ meta and para positions‚ with benzaldehyde as the control. Each of the four aldehydes reacted with (carbethoxymethylene) triphenylphosphorane to produce ethyl cinnamate‚ ethyl-3-(2-nitrophenyl)acrylate
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Perceptual Map Situation Analysis The Situation Analysis will help your company understand current market conditions and how the industry will evolve over the next eight years. The analysis can be done as a group or you can assign parts to individuals and then report back to the rest of the company. An online version of the Situation Analysis is available in the Getting Started area. (customers want better performing products) and for size is -0.7 (customers want smaller products). At the end of
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