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An anticlinorium is a large anticline in which a series of minor anticlinal folds are superimposed. Examples include the Late Jurassic to Early Cretaceous Purcell Anticlinorium in British Columbia [1] and the Blue Ridge anticlinorium of northern Virginia and Maryland in the Appalachians, [6] or the Nittany Valley in central Pennsylvania.
A mnemonic is a memory aid used to improve long-term memory and make the process of consolidation easier. Many chemistry aspects, rules, names of compounds, sequences of elements, their reactivity, etc., can be easily and efficiently memorized with the help of mnemonics.
is an alkaline solution of potassium permanganate; used in organic chemistry as a qualitative test for the presence of unsaturation, such as double bonds; N-Bromosuccinimide: used in radical substitution and electrophilic addition reactions in organic chemistry. Also acts as a mild oxidizer to oxidize benzylic or allylic alcohols.
A river anticline is a geologic structure that is formed by the focused uplift of rock caused by high erosion rates from large rivers relative to the surrounding areas. [1] An anticline is a fold that is concave down, whose limbs are dipping away from its axis, and whose oldest units are in the middle of the fold. [ 2 ]
Structure of iodine heptafluoride, an example of a molecule with the pentagonal-bipyramidal coordination geometry. In chemistry, a pentagonal bipyramid is a molecular geometry with one atom at the centre with seven ligands at the corners of a pentagonal bipyramid. A perfect pentagonal bipyramid belongs to the molecular point group D 5h.
In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR).The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.
The rule states that with the addition of a protic acid HX or other polar reagent to an asymmetric alkene, the acid hydrogen (H) or electropositive part gets attached to the carbon with more hydrogen substituents, and the halide (X) group or electronegative part gets attached to the carbon with more alkyl substituents.
In chemistry, an open-chain compound (or open chain compound) or acyclic compound (Greek prefix α 'without' and κύκλος 'cycle') is a compound with a linear structure, rather than a cyclic one. [1] An open-chain compound having no side groups is called a straight-chain compound (also spelled as straight chain compound).
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