Aldehydes are less sterically hindered than ketones. Also, aldehydes have fewer electron donating groups (EDG's) which can stabilize an electron-poor area. The extra carbon chain that ketones have that aldehydes do not have are the reason for both of these things. The neighboring carbon to the carbonyl carbon is an EDG and the carbon chain causes steric hindrance.
magnesium is most reactive
M. Norret has written: 'Synthetic approaches towards enantiopure axially-symmetric cyclic ketones and related compounds'
Elemental carbon is not particularly reactive towards acids in general.
pyrrole is more reactive towards electrophillic aromatic substiotution because it is able to stabilize the +ve charge of the intermediate carbocation
all of the halogens: bromine, fluorine, oxygen, chlorine and iodine. and it is highly reactive with water.
Sp hybridized carbon atom of alkyne pulls the electrons more strongly making he attached Hydrogen atom slightly acidic Becoming more suitable for Nucleophilic attack.In Alkenes no acidic Hydrogen is present.
No. Education requires an understanding that by doing something you will achieve a particular result. It is a proactive response. All plants are reactive. They do not grow towards where the sun will be, they towards where the sun is.
Its formula is Na3P. This is highly basic and very reactive towards acids (even as weak as water)
Because it is a polar solvent and highly reactive towards Grignard's reagent forming the alkanes.
Among these calcium is highly reactive towards acids.
Yes, they are highly reactive towards each other and their reactions are completed within 0.000001 seconds.
lithium is IA group element .As lithium is basic it should give its electron easily but it is not that effecient in this as sodium.As it has small radius and high nuclear attraction towards its electrons.but sodium has larger atomic radii than the lithium less nuclear attraction towards its electrons.thus sodium is more reactive than lithium.