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  2. organic chemistry - How to wedge d/hash notation a …

    WEBJul 27, 2017 · Using wedges and dashes, equally provides this information; however informs the reader about the sterochemical …

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    • What are the meanings of dotted and wavy lines in structural …

    • Hash and Wedge nomenclature - Chemistry Stack …

      WEBMay 24, 2017 · One of the first things learnt in organic chemistry is that wedged bonds can be thought of as bonds coming out of the plane of …

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      • organic chemistry - Different types of bond …

        WEBJun 11, 2023 · Partial bond in plain of paper or of unspecified stereochemistry. Also represents hydrogen bonds. Also represents …

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        • Does the 3D structure generated with MolView violate the wedge …

        • Does the Location of Line-Dash-Wedge Notations …

          WEBMar 23, 2019 · In Line-Dash-Wedge notation, when illustrating that an atom or bond is directed towards or away from the viewer (solid triangle for coming forward, dotted lines for going back), does the location of …

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        • Do you assume undrawn hydrogens are pointing …

          WEBJul 23, 2018 · Better practice is to indicate a specific stereochemistry explicitly, if you know or specifically presume it. In the molecule presented you could, of course, do this by drawing the methyl group with a …

        • Fischer projections - Chemistry Stack Exchange

          WEBSep 18, 2018 · This depiction tries to show how 3D tetrahedral structure is projected onto the paper plane, so the structure above is not meant to be a formula but a 3D model. Try to imagine you look at the structure …

        • Correct way of drawing D-configuration with this …

          WEBOct 21, 2016 · Swap the bold wedge and the dashed wedge. That will reverse the stereochemistry. Remember to do it for every position. This particularly important for something like isoleucine. – Zhe Oct 21, 2016 …

        • organic chemistry - How do I define the stereochemical …

        • organic chemistry - Conversion of molecular …

          WEBJul 5, 2020 · In general terms, if you start with a wedge-and-dash representation with the molecule in horizontal orientation, the substituents pointing towards you will end up on alternate sides of the Fischer …

        • How to convert wedge–dash structure into Fischer projection?

        • organic chemistry - How to determine the stereochemistry after ...

        • R and S Configuration Understanding - Chemistry Stack Exchange

        • organic chemistry - Determining R-S configuration with lowest …

        • organic chemistry - Determining R and S configuration for a cyclic ...

        • organic chemistry - How to draw Fischer projections for carbon …

        • Determining absolute configuration when the lowest priority group …

        • stereochemistry - Diastereomers - cyclic compounds - Chemistry …

        • organic chemistry - Can wedge and dash bonds on 1, 2 position of ...

        • Chiral center or not? Similar substituents, but still two possible ...

        • stereochemistry - How to draw wedged double bond in …

        • stereochemistry - Number of stereoisomers of trisubstituted ...