Answer:
I think its homogeneous
Explanation:
because its all pig, just different parts of the pig
I believe the correct answer from the choices listed above is option A. <span>A forward reaction in which adding heat decreases product formation is exothermic, while a forward reaction in which adding heat increases product formation is endothermic. Exothermic would mean that heat is being released by the process while the opposite is called endothermic in which it absorbs heat.</span>
Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.
Answer:
c. salty.
Explanation:
From the question,
The reaction of an acid , i.e hydrochloric acid and a base i.e. , sodium hydroxide takes place , which is a type of neutralization reaction,
Where the acid and a base reacts to give salt along with water .
From the question,
The reaction is as follows -
2 HCl + NaOH → NaCl + H₂O
Hence, the resulting product is a salt ,
Therefore , the resulting solution would taste like salt.
give brainliest pls thanksss
