under a strain - definizione. Che cos'è under a strain
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Cosa (chi) è under a strain - definizione

TYPE OF STRAIN ENERGY IN ORGANIC CHEMISTRY
A-1,3-strain

Strain gauge         
  • digital image correlation]] on a material testing coupon showing moving strain structures called [[Lüders band]]s
  • Geometries of strain gauges
  • An unmounted resistive foil strain gauge
ELECTRONIC COMPONENT
Strain gage; Strain Gauge; Crack gauge; Crack width gauge; Strain gauges; Molecular strain gauge
A strain gauge (also spelled strain gage) is a device used to measure strain on an object. Invented by Edward E.
strain gauge         
  • digital image correlation]] on a material testing coupon showing moving strain structures called [[Lüders band]]s
  • Geometries of strain gauges
  • An unmounted resistive foil strain gauge
ELECTRONIC COMPONENT
Strain gage; Strain Gauge; Crack gauge; Crack width gauge; Strain gauges; Molecular strain gauge
¦ noun a device for indicating the strain of a material or structure at the point of attachment.
Stress–strain curve         
  • The difference between true stress–strain curve and engineering stress–strain curve
  • Stress–strain curve for brittle materials compared to ductile materials
CURVE WHICH REPRESENTS THE DEFORMATION CAUSED BY A FORCE
Yield curve (physics); True stress; Stress-strain relations; Stress-strain curve; Stress and strain; Stress strain curve
In engineering and materials science, a stress–strain curve for a material gives the relationship between stress and strain. It is obtained by gradually applying load to a test coupon and measuring the deformation, from which the stress and strain can be determined (see tensile testing).

Wikipedia

Allylic strain

Allylic strain (also known as A1,3 strain, 1,3-allylic strain, or A-strain) in organic chemistry is a type of strain energy resulting from the interaction between a substituent on one end of an olefin (a synonym for an alkene) with an allylic substituent on the other end. If the substituents (R and R') are large enough in size, they can sterically interfere with each other such that one conformer is greatly favored over the other. Allylic strain was first recognized in the literature in 1965 by Johnson and Malhotra. The authors were investigating cyclohexane conformations including endocyclic and exocylic double bonds when they noticed certain conformations were disfavored due to the geometry constraints caused by the double bond. Organic chemists capitalize on the rigidity resulting from allylic strain for use in asymmetric reactions.