No I wouldn’t be the same
Option C coz it should be ( CNH4)2. Hope i cleared your doubt
Answer:
IV
Explanation:
The complete question is shown in the image attached.
Let us call to mind the fact that the SN1 mechanism involves the formation of carbocation in the rate determining step. The order of stability of cabocations is; tertiary > secondary > primary > methyl.
Hence, a tertiary alkyl halide is more likely to undergo nucleophilic substitution reaction by SN1 mechanism since it forms a more stable cabocation in the rate determining step.
Structure IV is a tertiary alkyl halide, hence it is more likely to undergo nucleophilic substitution reaction by SN1 mechanism.
Answer:
The scientific laws have been well proven before they are published so it is difficult to prove mistakes
Explanation:
Answer:
The electron pair geometry is Trigonal planar
Molecular geometry - Bent
Approximate bond angle - <120°
Explanation:
The valence shell electron pair repulsion theory enables us to predict the shapes of molecules based on the number of electron pairs present on the valence shell of the central atom and based on the hybridization state of the central atom.
sp2 hybridization corresponds to trigonal planar geometry. Let us recall that the presence of lone pairs causes a deviation of the molecular geometry from the expected geometry based on the number of electron pairs.
Hence, owing to one lone pair present, the observed molecular geometry is bent.