Rotation about C-C single bonds allows a compound to adopt a variety of . conformations configurations formations isomers projections are often used to draw the various conformations of a compound. conformations are lower in energy, while conformations are higher in energy. The difference in energy between staggered and eclipsed conformations of ethane is referred to as strain. strain occurs in cycloalkanes when bond angles deviate from the preferred °. The conformation of cyclohexane has no torsional strain and very little angle strain. The term "ring flip" is used to describe the conversion of one conformation into the other. When a ring has one substituent the equilibrium will favor the chair conformation with the substituent in the position.

Conformation

Explanation:

Conformation refers to "any of the spatial arrangements which the atoms in a molecule may adopt and freely convert between, especially by rotation about individual single bonds"(Oxford dictionary).

Carbon-Carbon single bonds are known to undergo rotations about its axis. These rotations leads to various conformations. The energy difference between conformations may be low or high depending on the structure of the molecule. The difference in energy between conformations determines a molecules's preferred conformation.

the formula would be mgso4

mgso[subscript]4

the mantle

explanation:

earth is divided into three layers: the crust or the outermost layer on which we live; the underlying, middle layer - the mantle - and the core (the innermost layer of earth).