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During the reading time, students may read the prompts and examine the documents. They may use this time to make notes, or begin writing their essay. The synthesis prompt typically requires students to consider a scenario, then formulate a response to a specific element of the scenario using at least three of the accompanying sources for ...
Synthetic phonics, also known as blended phonics or inductive phonics, [1] is a method of teaching English reading which first teaches letter-sounds (grapheme/phoneme correspondences) and then how to blend (synthesise) these sounds to achieve full pronunciation of whole words.
Many retrosynthetic disconnections important for organic synthesis planning use carbocationic synthons. Carbon-carbon bonds, for example, exist ubiquitously in organic molecules, and are usually disconnected during a retrosynthetic analysis to yield carbocationic and carbanionic synthons.
In computer science, program synthesis is the task to construct a program that provably satisfies a given high-level formal specification.In contrast to program verification, the program is to be constructed rather than given; however, both fields make use of formal proof techniques, and both comprise approaches of different degrees of automation.
Total synthesis, the complete organic synthesis of complex organic compounds, usually without the aid of biological processes; Convergent synthesis or linear synthesis, a strategy to improve the efficiency of multi-step chemical syntheses; Dehydration synthesis, a chemical synthesis resulting in the loss of a water molecule
In polymer chemistry, ring-opening metathesis polymerization (ROMP) is a type of chain-growth polymerization involving olefin metathesis. [1] The reaction is driven by relieving ring strain in cyclic olefins. [2]
For example, according to Best Friends Network staff, cats can exist with barely noticeable behavioral changes as their loss of sight comes on gradually. As they start losing vision, felines begin ...
In the cited example the Lewis acid TiCl 4 is used. First, the Lewis acid activates the aldehyde component followed by carbon-carbon bond formation between the enol silane and the activated aldehyde. With the loss of a chlorosilane the compound 1 is built. The desired product, a racemate of 2 and 3, is obtained by aqueous work-up. [3]