Here we have to explain and predict the product of the reaction between hept-3-yne and bromine (Br₂)
The reaction between hept-3-yne and bromine produces <em>trans</em>-3,4-dibromo-3-heptene.
The reaction between the unsaturated hydrocarbon with halogen remove the unsaturation in the molecule and produces di halo compound. The reaction proceed through the formation of bromonium ion.
In this reaction as the unsaturation present in the middle of the alkyl chain i.e. hept-3-yne. The reaction will stop after the formation of di-halo compound with one double bond as shown in the figure.
The product will be exclusively trans product as the bromine is a bulky group and the formation of bromonium ion (intermediate) will be one side of the unsaturated compound.
Answer & Explanation:
The law of multiple proportion states that two elements A and B can react with each other to form multiple compounds while one of the two elements remain fixed.
For Example
Hydrogen reacts with oxygen to form:
Water (H2O)
Hydrogen peroxide (H2O2)
Answer:
As the world changes, plants and animals change with it. Aside from a few living fossils, the species we see today are very different from species that lived in the past. Thus, the fossil record can be used to show that organisms changed to meet new conditions. This is the result of evolution of species over time.
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Explanation:
Answer: The Lewis structure of Chloroacetate can be found at the attachment below.
Explanation:
CH2ClCOO- The chemical compound is called Chloroacetate.
Reference link for the Chloroacetate structure.
https://www.google.com/search?q=lewis+structure+for+CH2ClCOO-&prmd=ivn&sxsrf=ALeKk03mQcLiY-q5pEriMR0_26ZTXLjmJg:1589680325594&source=lnms&tbm=isch&sa=X&ved=2ahUKEwjfxPPY5LnpAhVloXEKHeAwD-wQ_AUoAXoECA4QAQ&cshid=1589680746615&biw=360&bih=559&dpr=3#
