How many of thc following compounds could serve as Bronsted-Lowy acid?ChlOHNaHSo4Ollehrotlueefour...

How could you synthesize the following compounds starting with a carboxylic acid?

Okay. So I want to create the following compounds using no more than for carbons. And in the first one we have the structure. So this can be created through a deal's alter action. This is a good way to create six carbon rings with different functional groups. And this involves a dying which is known as the it's gonna be a liquid fire are the equivalent to it. And this is reacting with the dye in the fall. So in this case we need two carbons sticking 20.6 carbon ring. Also another carbon for the alcohol and 23 carbons. We also put you also want to put an electron with your own group on the diana file to make it more reactive. So this is similar to putting electron withdrawing groups on electra files because they make the the um how did the carbon carbon or it just makes them more reactive. And this is going to attack is carbon. As a result, it's gonna attack here. And foreign born right there. Suite of six Carbon Ring and carbon six. This is 1, 2 34 five at six Covered six attached the Alga Hood ends can be reduced to a primary alcohol with suiting for hydro and water. See our products okay, For B. We have just an arcane. Okay, so again, starting with the dying and then we would add A two Carbon Ring. So first we need two carbons to complete V six Carbon chain and opposite tomorrow here. So I need four in total. And I'm gonna use it at all to hide again because it's easy to reduce to an alcohol and then dehydrate the alcohol to an arcane. So you're gonna have an alpha beta unsaturated cartoon, I mean alphabet to unsaturated alcohol. So attacking right there. This is going to attack right here. So carbon six is attached to a four carbon at a hood and we're gonna use the same reaction in a turning into an alcohol and then dehydrating the alcohol with sulfuric acid or some of their strong acid. And with you, too. So we get Naquin and then we're gonna reduce, yeah, keane with hydrogen and platinum final products.

Hi everyone. So in this question they asked named the following acid salt, its cage and so forth. That is position by sulfate protection. Bye. Some friend Then LIHS- 03 lithium bison self fight lithium my sulfide, the team by sulfide When BBH Air so forth. So laid by Arsene lad. Bye. I was selling. I was a nipper. Thanks lot.

To name this compound. Let's highlight the longest carbon chain, including the double bond, which will be this chain here. That's the parent chain. Let's number that parent chain giving the double bond the lowest possible numbers. Starting from the left Carbon one, too. Three before 5678 The parents is Oct. There's a double bond, which begins at carbon two. I mean, there is to substitute, since there is a to carbon substitution attached to carbon four. This is a four Ethel, and there is a one carbon substitute attached to carbon five. Say five methyl. Let's start with the name. Putting this all together. We'll start with substitutes alphabetically. Four. Dash fo Dash five dash Methanol two dash our team.

The longest carbon sheen containing the alcohol functional group will be this change. Here, we're gonna number this carbon chain giving the alcohol group of lowest possible numbers starting from carbon one, 23 4567 eight, nine The parents is known This is all single bonds. So the suffix is a N e. And there's alcohol at carbon three sorts of three dash Oh, l There is a vey substitue INTs at carbon four, which is a two carbon chain. It's a four Ethel group, starting with the Group four Dash F Ool dash. Now we're gonna name yuck! Hole three. Yeah, non and all.