Answer:
Ether
SN1 mechanism
Explanation:
The nucleophile in this reaction is CH3OH. It is a poor nucleopile. We already know that a poor nucleophile reacting with a tertiary alkyl halide often leads to the substitution product as the major product.
Also, the iodide ion is a good leaving group. This makes the SN1 substitution more likely yielding the ether as the major product as shown in the image attached.
Answer: Heres the answers
Explanation:
Answer:
The first option.
Explanation:
Warm solvent and stirring promote quick dissolving . Also with small crystals more of the surface is in contact with the solvent than with large crystals.
Answer:
The substance that remained on the filter paper is Al(OH).
Explanation:
- Filter paper is the substance that is used in laboratory to separate the solid objects. It doesn't filter aqueous and gaseous products.
- So in our experiment the product formed is aluminum hydroxide Al(OH) and sodium chloride (NaCl).
- Between two products, sodium chloride is in aqueous form as indicated in the question. So it wont remain in the filter paper.
- Hence aluminum hydroxide being only solid product remains on the filter paper.
